Surgyco STF00710
by Surgyco LLC
Surgyco STF00710 is a Class II device made by Surgyco LLC, cleared under FDA 510(k) K082815 on 8 Oct 2008 and listed in FDA GUDID since 20 Dec 2024 (UDI-DI 10850053289795), 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 | Number10850053289795 | Date20 Dec 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK082815 | Date8 Oct 2008 | StatusActive |
Official records
- AccessGUDID record 10850053289795
- FDA 510(k) database K082815
Across registries
- FDA 510(k) K082815 decided 8 Oct 2008 Active
- FDA GUDID UDI-DI 10850053289795 listed 20 Dec 2024 Listed
Timeline
- Cleared FDA 510(k) K082815
- Listed FDA GUDID 10850053289795
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Surgyco
- Generic name
- General-purpose syringe, single-use
- Model / reference
- STF00710
- Primary DI / UDI-DI
- 10850053289795
- 510(k) Number
- FDA product code
- EZL
- GMDN term
- General-purpose syringe, single-use
- Device class
- Class II
- Regulation number
- 876.5130
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under General-purpose syringe, single-use.