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Tekno® 50459-16

by Tekno Medical Optik-Chirurgie GmbH & Co.

Tekno® 50459-16 is a Class I device made by Tekno Medical Optik-Chirurgie GmbH & Co., listed in FDA GUDID since 20 Nov 2025 (UDI-DI 04044684066392), 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 Number04044684066392 UDI-DI Date20 Nov 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  • Withdrawn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
Tekno®
Generic name
Surgical soft-tissue manipulation forceps, alligator, reusable
Model / Ref / Catalog
50459-16
Primary DI / UDI-DI
04044684066392
FDA product code
KAE
GMDN term
Surgical soft-tissue manipulation forceps, alligator, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code KAE (Forceps, Ent).

Other devices from Tekno Medical Optik-Chirurgie GmbH & Co.

See all devices from Tekno Medical Optik-Chirurgie GmbH & Co. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)