Surgyco 010-VPSB25G2
by Surgyco LLC
Surgyco 010-VPSB25G2 is a Class II device made by Surgyco LLC, cleared under FDA 510(k) K230080 on 7 Jul 2023 and listed in FDA GUDID since 23 Dec 2025 (UDI-DI 10850074089084), 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 | Number10850074089084 | Date23 Dec 2025 | StatusListed |
| United States | FDA 510(k) | NumberK230080 | Date7 Jul 2023 | StatusActive |
Official records
- AccessGUDID record 10850074089084
- FDA 510(k) database K230080
Across registries
- FDA 510(k) K230080 decided 7 Jul 2023 Active
- FDA GUDID UDI-DI 10850074089084 listed 23 Dec 2025 Listed
Timeline
- Cleared FDA 510(k) K230080
- Listed FDA GUDID 10850074089084
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- Withdrawn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
- 010-VPSB25G2
- Description
- VeinPulse Safety Slide Blood Collection Set 25G x 3/4"
- Primary DI / UDI-DI
- 10850074089084
- 510(k) Number
- FDA product code
- JKA
- GMDN term
- General-purpose syringe, single-use
- Device class
- Class II
- Regulation number
- 862.1675
- GUDID distribution status
- In Commercial Distribution
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