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Inami & Co., Ltd. S-325

by Diamatrix

Inami & Co., Ltd. S-325 is a Class I device made by Diamatrix, listed in FDA GUDID since 20 Oct 2025 (UDI-DI 00810163790478), 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 Number00810163790478 UDI-DI Date20 Oct 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  • Withdrawn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
Inami & Co., Ltd.
Generic name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Model / Ref / Catalog
S-325
Primary DI / UDI-DI
00810163790478
FDA product code
HNR
GMDN term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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)