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Nanocut S15002

by Aurolab

Nanocut S15002, an ophthalmic knife (FDA Class I; FDA product code HNN, Knife, Ophthalmic) made by Aurolab, was listed in FDA GUDID on 15 Jun 2023 (UDI-DI 10803878036341); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number10803878036341 UDI-DI Date15 Jun 2023ListedStatusListed GUDID: not 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  • Withdrawn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
Nanocut
Generic name
Ophthalmic knife, single-use
Model / reference
S15002
Primary DI / UDI-DI
10803878036341
FDA product code
HNN
GMDN term
Ophthalmic knife, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code HNN (Knife, Ophthalmic).

Other devices from Aurolab

See all devices from Aurolab →

Properties

  • Supplied sterile
  • Single use
  • Contains latex
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)