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Diamatrix F355S

by Diamatrix

Diamatrix F355S is a Class I device made by Diamatrix, listed in FDA GUDID since 1 Feb 2021 (UDI-DI 00813059017079), 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 Number00813059017079 UDI-DI Date1 Feb 2021ListedStatusListed 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  • Withdrawn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
Diamatrix
Generic name
Ophthalmic implant handling forceps, reusable
Model / Ref / Catalog
F355S
Description
Implant Removal Forceps, Flat serrated jaws with sharp activation pin on bottom jaw, Scissor-action Flat serrated handle, 120mm Overall Length, Stainless Steel
Primary DI / UDI-DI
00813059017079
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
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Ophthalmic implant handling forceps, reusable

Other devices from Diamatrix

See all devices from Diamatrix →

Properties

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