Complete List of FDA Authorized Vapes in 2026
As of May 5, 2026, the U.S. Food and Drug Administration lists 45 e-cigarette products that have received federal marketing authorization.
These 45 products are the only e-cigarettes that the FDA says may currently be lawfully sold in the United States. The list includes devices, pods, cartridges and e-liquid packages from five manufacturers:
- Glas Inc.
- JUUL Labs Inc.
- Logic Technology Development LLC
- NJOY LLC
- R.J. Reynolds Vapor Company
The number 45 does not mean American consumers can choose from 45 different vape devices. The FDA counts each device, pod, cartridge, flavor and nicotine strength as a separate authorized product.
Several products on the regulatory list may also have been discontinued or may be difficult to find commercially. FDA authorization and current retail availability are two different questions.
Quick Answer: How Many Vapes Has the FDA Authorized?
The FDA lists 45 authorized e-cigarette products as of May 5, 2026. These include devices and product-specific refills—not 45 separate vape systems. They are the only e-cigarettes the FDA currently identifies as lawful for sale in the United States.
The latest additions are four 50 mg/mL Glas G2 pods:
- Classic Menthol
- Fresh Menthol
- Gold
- Sapphire
The FDA describes Gold and Sapphire as its first authorized e-cigarette products with flavors other than tobacco or menthol.
FDA-Authorized Vape Brands at a Glance
| Manufacturer | Authorized product records |
|---|---|
| Glas Inc. | 6 |
| JUUL Labs Inc. | 5 |
| Logic Technology Development LLC | 8 |
| NJOY LLC | 10 |
| R.J. Reynolds Vapor Company | 16 |
| Total | 45 |
The total includes hardware units and consumable refills.
What Does FDA Authorization Mean?
Most new tobacco products must receive a written FDA marketing order before they can legally be introduced into interstate commerce in the United States.
E-cigarette manufacturers generally seek authorization through the Premarket Tobacco Product Application pathway.
When reviewing a PMTA, the FDA considers whether marketing the product would be “appropriate for the protection of the public health.”
The review may include:
- Product ingredients
- Aerosol chemistry
- Toxicology
- Nicotine delivery
- Adult smoking-switching potential
- Youth-use risks
- Product design
- Marketing plans
- Consumer behaviour
- Population-level effects
Receiving a marketing granted order allows the specific product to be marketed under the conditions imposed by the FDA.
It does not mean that the FDA considers the product safe.
Updated FDA Authorized Vape List
The following list is based on the FDA’s official authorized e-cigarette page.
Glas G2 Authorized Products
Glas has six products on the FDA list.
Device
- Glas G2 Device
Authorized Glas G2 Pods
- Glas G2 Blonde Tobacco 50 mg/mL Pod
- Glas G2 Gold 50 mg/mL Pod
- Glas G2 Fresh Menthol 50 mg/mL Pod
- Glas G2 Sapphire 50 mg/mL Pod
- Glas G2 Classic Menthol 50 mg/mL Pod
All five authorized pods contain 50 mg/mL—or 5%—tobacco-derived nicotine.
Glas Authorization Timeline
On March 12, 2026, the FDA authorized:
- Glas G2 Device
- Blonde Tobacco 50 mg/mL Pod
On May 5, 2026, the FDA authorized four additional pods:
- Classic Menthol
- Fresh Menthol
- Gold
- Sapphire
The FDA describes Gold and Sapphire as non-tobacco, non-menthol flavors. Industry reporting identifies them as fruit-flavored products, but retailers should use the exact authorized product names when checking compliance.
Why the Glas Decision Was Significant
The May 5 orders marked the first time the FDA authorized e-cigarette products with flavors other than tobacco or menthol.
According to the FDA, the Glas system uses age-verification and device-access technology intended to reduce youth use.
The system requires an adult user to:
- Verify age and identity with a government-issued ID.
- Pair the device with a smartphone through Bluetooth.
- Keep the verified smartphone near the device.
- Complete random biometric checks.
The FDA said non-tobacco-flavored products may receive authorization when an application demonstrates that the expected benefit to adults who smoke outweighs the risks, including potential youth use.
The four May authorizations apply only to the named Glas pods. They do not authorize every Glas product or flavored e-cigarettes generally. FDA Glas announcement
JUUL Authorized Products
The FDA has authorized the JUUL device and four refill pods.
Device
- JUUL Device
Virginia Tobacco Pods
- JUULpods Virginia Tobacco 3.0%
- JUULpods Virginia Tobacco 5.0%
Menthol Pods
- JUULpods Menthol 3.0%
- JUULpods Menthol 5.0%
The FDA issued the JUUL marketing granted orders on July 17, 2025.
The authorization applies only to these four pod variants. It does not cover previously sold JUUL flavors such as mango, fruit, crème or cucumber.
Logic Authorized Products
The FDA list contains eight Logic product records.
Logic Pro Products
- Logic Pro Capsule Tank System (1)
- Logic Pro Capsule Tank System (2)
- Logic Pro Tobacco e-Liquid Package
Logic Power Products
- Logic Power Rechargeable Kit
- Logic Power Tobacco e-Liquid Package
Logic Vapeleaf Products
- Logic Vapeleaf Tobacco Vapor System
- Logic Vapeleaf Cartridge/Capsule Package
Additional Logic Cartridge
- Logic Regular Cartridge/Capsule Package
Some names on the FDA list refer to product configurations or versions that may appear nearly identical to consumers.
Is Logic Vapeleaf an E-Cigarette?
The FDA includes Logic Vapeleaf on its authorized ENDS list, but it differs from a conventional e-liquid vape.
Logic Vapeleaf uses a solid tobacco-containing capsule rather than ordinary bottled e-liquid. It can therefore be described as a tobacco-vapor or heated-tobacco-style system.
This illustrates a limitation of the FDA’s public list: its regulatory grouping does not always match the product categories used by consumers and retailers.
Retailers should rely on the official product name and marketing order rather than assuming every listed product is a conventional liquid-based e-cigarette.
NJOY Authorized Products
The FDA lists ten NJOY products.
NJOY DAILY Products
- NJOY DAILY Rich Tobacco 4.5%
- NJOY DAILY Menthol 4.5%
NJOY DAILY EXTRA Products
- NJOY DAILY EXTRA Rich Tobacco 6%
- NJOY DAILY EXTRA Menthol 6%
NJOY ACE Device
- NJOY ACE Device
NJOY ACE Tobacco Pods
- NJOY ACE Pod Classic Tobacco 2.4%
- NJOY ACE Pod Classic Tobacco 5%
- NJOY ACE Pod Rich Tobacco 5%
NJOY ACE Menthol Pods
- NJOY ACE Pod Menthol 2.4%
- NJOY ACE Pod Menthol 5%
The FDA authorized the NJOY ACE menthol pods and NJOY DAILY menthol products on June 21, 2024.
Before the Glas decision, those orders represented the FDA’s first authorization of menthol-flavored e-cigarette products.
Vuse Authorized Products
R.J. Reynolds Vapor Company has 16 product records on the FDA’s list. These cover Vuse Alto, Vuse Solo, Vuse Vibe and Vuse Ciro.
Vuse Alto Products
Device
- Vuse Alto Power Unit
Golden Tobacco Pods
- Vuse Alto Pod Golden Tobacco 1.8%
- Vuse Alto Pod Golden Tobacco 2.4%
- Vuse Alto Pod Golden Tobacco 5%
Rich Tobacco Pods
- Vuse Alto Pod Rich Tobacco 1.8%
- Vuse Alto Pod Rich Tobacco 2.4%
- Vuse Alto Pod Rich Tobacco 5%
The FDA issued marketing granted orders for the Vuse Alto device and six tobacco-flavored pods on July 18, 2024.
The authorization does not cover Vuse Alto menthol or mixed-berry pods.
Vuse Solo Products
- Vuse Solo Power Unit
- Vuse Replacement Cartridge Original 4.8% G1
- Vuse Replacement Cartridge Original 4.8% G2
The FDA counts the two cartridge versions as separate authorized products.
For consumers, the differences between product generations may be relatively minor. For legal compliance, however, each marketing order is product-specific.
Vuse Vibe Products
- Vuse Vibe Power Unit (1)
- Vuse Vibe Power Unit (2)
- Vuse Vibe Tank Original 3.0%
The two power units represent separate regulatory product records, even if their user experience is similar.
Vuse Ciro Products
- Vuse Ciro Power Unit (1)
- Vuse Ciro Power Unit (2)
- Vuse Ciro Cartridge Original 1.5%
Vuse Ciro may no longer be widely available commercially, but its marketing orders remain part of the FDA’s official list.
This is why the number of FDA-authorized products should not be interpreted as the number of options a consumer can currently find in stores.
FDA Authorization Timeline
October 12, 2021: Vuse Solo
The FDA issued its first e-cigarette marketing granted orders for the Vuse Solo system and tobacco-flavored cartridges.
March 24, 2022: Logic
The FDA authorized several Logic Pro, Logic Power and Logic Vapeleaf products.
April 26, 2022: NJOY ACE
The NJOY ACE device and tobacco-flavored pods received marketing authorization.
May 12, 2022: Vuse Vibe and Ciro
The FDA authorized Vuse Vibe and Vuse Ciro hardware and tobacco-flavored refills.
June 10, 2022: NJOY DAILY
The agency authorized NJOY DAILY and NJOY DAILY EXTRA tobacco-flavored products.
June 21, 2024: NJOY Menthol Products
The FDA authorized:
- NJOY DAILY Menthol 4.5%
- NJOY DAILY EXTRA Menthol 6%
- NJOY ACE Menthol 2.4%
- NJOY ACE Menthol 5%
July 18, 2024: Vuse Alto
The FDA authorized the Vuse Alto power unit and six Golden Tobacco and Rich Tobacco pods.
July 17, 2025: JUUL
The agency authorized the JUUL device and four tobacco and menthol pods in 3% and 5% nicotine strengths.
March 12, 2026: Glas G2 System
The FDA authorized the Glas G2 device and Blonde Tobacco 50 mg/mL pod.
May 5, 2026: Four Additional Glas Pods
The FDA added:
- Gold 50 mg/mL
- Sapphire 50 mg/mL
- Classic Menthol 50 mg/mL
- Fresh Menthol 50 mg/mL
These orders increased the official total to 45.
Authorized Products Versus Available Products
FDA authorization does not guarantee that a product is:
- Still manufactured
- Still distributed
- Available nationwide
- Stocked by major retailers
- Commercially successful
- Permitted under every state law
A manufacturer may discontinue an authorized product without the FDA immediately removing its marketing order from the public list.
Therefore, websites publishing a “currently available” list should verify commercial availability separately.
A more accurate description is:
The FDA has authorized 45 e-cigarette product records, but the number of distinct systems currently available to consumers is substantially smaller.
How Many Distinct Vape Systems Are Represented?
The list represents approximately ten named systems:
- Glas G2
- JUUL
- Logic Pro
- Logic Power
- Logic Vapeleaf
- NJOY DAILY
- NJOY ACE
- Vuse Alto
- Vuse Solo
- Vuse Vibe
- Vuse Ciro
Logic Vapeleaf is not a conventional e-liquid system, while Vuse Ciro may no longer be widely marketed.
NJOY DAILY and NJOY DAILY EXTRA are separate disposable product configurations rather than refillable systems.
The exact number depends on whether different hardware generations and closely related product variants are counted separately.
Are Heated-Tobacco Products E-Cigarettes?
Heated-tobacco products and e-cigarettes are generally considered different product categories.
E-Cigarettes
E-cigarettes normally heat a liquid containing ingredients such as propylene glycol, vegetable glycerin, nicotine and flavorings.
Heated-Tobacco Products
Heated-tobacco products heat processed tobacco material without burning it in the same way as a cigarette.
IQOS is a well-known heated-tobacco system that has received FDA marketing authorization. However, IQOS products are not included on the FDA’s dedicated authorized e-cigarette webpage.
Logic Vapeleaf is included even though it uses a solid tobacco-containing capsule. This creates some inconsistency in how the public-facing list groups products.
For SEO and compliance content, it is better to discuss FDA-authorized e-cigarettes and FDA-authorized heated-tobacco products separately.
Are IQOS Products Part of the 45?
No. The FDA’s total of 45 on its authorized e-cigarette webpage does not include IQOS devices and HeatSticks.
IQOS has received separate FDA marketing orders as a heated-tobacco product. Some IQOS products have also received modified risk tobacco product authorization.
Adding IQOS products to an e-cigarette count would not match the FDA’s current public list.
Are FDA-Authorized Vapes “FDA Approved”?
No.
The correct term is FDA-authorized for marketing.
The FDA’s “safe and effective” approval standard for medicines does not apply to tobacco products. Instead, the agency determines whether marketing a new tobacco product is appropriate for the protection of public health.
The FDA explicitly warns that authorization does not mean:
- The product is safe
- The product is harmless
- The product is FDA approved
- The product is recommended for non-smokers
- The product is approved as a quit-smoking medicine
All authorized e-cigarettes remain potentially addictive, and people who do not currently use tobacco products should not start.
Acceptable and Misleading Terminology
| More accurate wording | Potentially misleading wording |
|---|---|
| FDA-authorized vape | FDA-approved vape |
| Received a marketing granted order | Certified safe by FDA |
| Authorized through the PMTA pathway | Approved smoking-cessation device |
| May be lawfully marketed | Harmless alternative |
| Specific authorized product | Entire brand approved |
Is an Unauthorized Vape Illegal?
Under the FDA’s current position, new e-cigarette products that lack the required written marketing authorization cannot be lawfully marketed in the United States.
The FDA states:
“These 45 products are the only e-cigarettes that may currently be lawfully sold in the U.S.”
A pending PMTA does not equal authorization.
Neither do claims such as:
- “PMTA submitted”
- “Application accepted”
- “Under scientific review”
- “FDA registered”
- “Made in an FDA-registered facility”
- “Pending litigation”
- “On the market before enforcement”
- “Not currently an enforcement priority”
Enforcement discretion and legal authorization are different concepts.
What About Products With Pending Applications?
Some products may have applications under review or ongoing court proceedings. Their procedural status can affect how and when the FDA takes enforcement action.
However, that does not automatically provide a marketing granted order.
Retailers should not interpret the absence of immediate enforcement as confirmation that a product is legally authorized.
The FDA states that unauthorized products may be subject to:
- Warning letters
- Civil money penalties
- Import detention
- Seizure
- Injunction
- Administrative action
- Civil enforcement
- Criminal enforcement
Distributors and retailers—not only manufacturers—may face enforcement consequences.
What Categories Remain Absent From the FDA List?
Despite the new Glas authorizations, the FDA list remains narrow compared with the broader U.S. vaping market.
The official list contains no authorized examples of:
- Bottled e-liquid
- Open-system vape tanks
- Rebuildable atomizers
- Independently bottled vape-shop e-liquid
- Most disposable vape brands
- Most fruit-flavored pods
- Most high-capacity disposable devices
- Most products sold by independent vape manufacturers
The May 2026 Glas decision created the first exceptions for non-tobacco and non-menthol flavored ENDS products.
However, those products use device-level age verification and are limited to the specific 50 mg/mL pods named in the marketing orders.
What Should Vape Retailers Do?
Check the Exact SKU
FDA authorization applies to specific products, not just a brand or product family.
For example, authorization for a JUUL Menthol 5% pod does not cover every JUUL-compatible pod.
Verify Nicotine Strength
Different nicotine strengths are separate products. One authorized strength does not automatically cover another.
Verify the Flavor
An authorized tobacco or menthol product does not make fruit products under the same brand legal.
Use the Official FDA Database
The FDA says its authorized e-cigarette webpage is the first place where new ENDS authorizations will appear.
Its searchable tobacco-products database provides more comprehensive product-level information.
Keep Supplier Records
Retailers should retain:
- Supplier invoices
- Product photographs
- UPC information
- Manufacturer details
- FDA marketing-order references
- Purchase dates
- Inventory records
Check State and Local Law
Federal authorization does not override:
- State flavor bans
- State product directories
- Local licensing requirements
- Excise taxes
- Packaging rules
- Retail display restrictions
- Age-verification requirements
A product can have federal marketing authorization and still be restricted in a particular state or city.
Frequently Asked Questions
How many e-cigarettes has the FDA authorized?
The FDA lists 45 authorized e-cigarette product records as of May 5, 2026. This total includes devices, pods, cartridges and e-liquid packages.
Are there 45 different vape devices?
No. Many of the 45 records are refill pods and cartridges. Others are duplicate or revised hardware versions.
Which vape brands are FDA-authorized?
The official list includes products made by Glas, JUUL, Logic, NJOY and R.J. Reynolds Vapor Company.
Has the FDA authorized fruit-flavored vapes?
Yes. On May 5, 2026, the FDA authorized two Glas G2 pods described as non-tobacco and non-menthol products. They are sold under the names Gold and Sapphire.
Are disposable vapes authorized?
The NJOY DAILY and NJOY DAILY EXTRA products are closed disposable e-cigarettes. Most disposable vape brands sold in the broader U.S. market have not received FDA authorization.
Has the FDA authorized bottled e-liquid?
No bottled e-liquid appears on the FDA’s current authorized e-cigarette list.
Are open-system vape devices authorized?
The FDA’s current list does not include conventional open-system tanks and refillable vape-shop devices.
Is JUUL legal in the United States?
The JUUL device and four specific Virginia Tobacco and Menthol pods received marketing authorization in July 2025. Other JUUL flavors are not covered.
Is Vuse Alto FDA-authorized?
The Vuse Alto power unit and six Golden Tobacco and Rich Tobacco pods are authorized. Menthol, berry and other Alto variants are not included.
Does a submitted PMTA make a vape legal?
No. Submission or acceptance of an application is not the same as receiving a written marketing granted order.
Are FDA-authorized vapes safe?
No tobacco product is safe. FDA authorization means the product met the applicable public-health standard for marketing; it is not a safety approval.
How often does the FDA list change?
The FDA says it intends to update its authorized e-cigarette webpage on the day it issues a new authorization. Publishers and retailers should check the official page regularly.
Final Conclusion
The FDA’s authorized e-cigarette list expanded to 45 product records on May 5, 2026, following the authorization of four additional Glas G2 pods.
The list now contains products from Glas, JUUL, Logic, NJOY and R.J. Reynolds. It includes tobacco, menthol and—for the first time—two non-tobacco, non-menthol Glas products.
However, the headline number requires context. Most of the 45 entries are pods, cartridges or separate hardware versions rather than distinct vape systems. Some authorized products may also no longer be widely available.
Retailers should verify the exact product name, flavor and nicotine strength rather than assuming an entire brand is authorized.
Most importantly, a pending PMTA, lawsuit or low enforcement priority does not equal legal marketing authorization. Under the FDA’s current position, only the 45 products on its authorized ENDS list may presently be lawfully sold as e-cigarettes in the United States.
Compliance disclaimer: This article provides general regulatory information and does not constitute legal advice. Product status and enforcement policies can change. Always verify products against the current FDA database.
