Vortex Surgical Inc VS0740.23
Vortex Surgical Inc VS0740.23 is an ophthalmic soft-tissue manipulation forceps (FDA Class I; FDA product code HNR, Forceps, Ophthalmic) made by Vortex Surgical, Inc., listed in FDA GUDID since 1 Feb 2023 (UDI-DI 00810123481538), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00810123481538 | Date1 Feb 2023 | StatusListed |
Official records
- AccessGUDID record 00810123481538
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vortex Surgical Inc
- Generic name
- Ophthalmic soft-tissue manipulation forceps, probe-like, single-use
- Model / reference
- VS0740.23
- Primary DI / UDI-DI
- 00810123481538
- FDA product code
- HNR
- GMDN term
- Ophthalmic soft-tissue manipulation forceps, probe-like, single-use
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- In Commercial Distribution
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