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Vortex Surgical Inc. VS0753.27

by Vortex Surgical, Inc.

Vortex Surgical Inc. VS0753.27 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 18 Apr 2025 (UDI-DI 00810123482818), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810123482818 UDI-DI Date18 Apr 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Vortex Surgical Inc.
Generic name
Ophthalmic soft-tissue manipulation forceps, probe-like, single-use
Model / reference
VS0753.27
Primary DI / UDI-DI
00810123482818
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

Related devices

Category: Ophthalmic soft-tissue manipulation forceps, probe-like, single-use

Similar devices in this category

Other devices filed under Ophthalmic soft-tissue manipulation forceps, probe-like, single-use.

Other devices from Vortex Surgical, Inc.

See all devices from Vortex Surgical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)