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Strabismus Scissors AS12-061

by Aurora Surgical LLC

Strabismus Scissors AS12-061 is a Class I device made by Aurora Surgical LLC, listed in FDA GUDID since 24 Jul 2023 (UDI-DI 08175700147514), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08175700147514 UDI-DI Date24 Jul 2023ListedStatusListed 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  • Withdrawn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
Strabismus Scissors
Generic name
Conjunctival scissors, reusable
Model / Ref / Catalog
AS12-061
Primary DI / UDI-DI
08175700147514
FDA product code
HNF
GMDN term
Conjunctival scissors, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Conjunctival scissors, reusable

Similar devices

Other devices filed under FDA product code HNF (Scissors, Ophthalmic).

Other devices from Aurora Surgical LLC

See all devices from Aurora Surgical LLC →

Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)