Oph.Forceps 08-01338

by Katena Products, Inc.

Oph.Forceps 08-01338 is a Class I device made by Katena Products, Inc., listed in FDA GUDID since 22 Nov 2022 (UDI-DI 00852979003892), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00852979003892 UDI-DI	Date22 Nov 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00852979003892

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Oph.Forceps
Generic name: Ophthalmic implant handling forceps, reusable
Model / Ref / Catalog: 08-01338

Primary DI / UDI-DI: 00852979003892
FDA product code: HNR
GMDN term: Ophthalmic implant handling forceps, reusable

Device class: Class I
Regulation number: 886.4350
GUDID distribution status: In Commercial Distribution

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Properties

Prescription use
Premarket exempt

Other properties (13, all answered No)