Deesse Pro Express TN19G
Deesse Pro Express TN19G (111B) is a Class II device made by iSMART Developments, Ltd., cleared under FDA 510(k) K191629 on 12 Sep 2019 and listed in FDA GUDID since 5 May 2021 (UDI-DI 05060534510395), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05060534510395 | Date5 May 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK191629 | Date12 Sep 2019 | StatusActive |
Official records
- AccessGUDID record 05060534510395
- FDA 510(k) database K191629
Across registries
- FDA 510(k) K191629 decided 12 Sep 2019 Active
- FDA GUDID UDI-DI 05060534510395 listed 5 May 2021 Listed
Timeline
- Cleared FDA 510(k) K191629
- Listed FDA GUDID 05060534510395
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Deesse Pro Express
- Generic name
- Cosmetic red-light phototherapy system, home-use
- Model / Ref / Catalog
- TN19G, 111B
- Primary DI / UDI-DI
- 05060534510395
- 510(k) Number
- FDA product code
- OHS
- GMDN term
- Cosmetic red-light phototherapy system, home-use
- Device class
- Class II
- Regulation number
- 878.4810
- GUDID distribution status
- In Commercial Distribution
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