Troposphere 1001528
Troposphere 1001528 is a Class II device made by Henry Schein, Inc., cleared under FDA 510(k) K951865 on 25 May 1995 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI H65810015281), 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 | NumberH65810015281 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK951865 | Date25 May 1995 | StatusActive |
Official records
- FDA 510(k) database K951865
Across registries
- FDA 510(k) K951865 decided 25 May 1995 Active
- FDA GUDID UDI-DI H65810015281 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K951865
- Listed FDA GUDID H65810015281
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Troposphere
- Generic name
- Dental amalgam
- Model / Ref / Catalog
- 1001528
- Primary DI / UDI-DI
- H65810015281
- 510(k) Number
- FDA product code
- EJJ
- GMDN term
- Dental amalgam
- Device class
- Class II
- Regulation number
- 872.3070
- GUDID distribution status
- In Commercial Distribution
- Size
- Weight — 400 Milligram