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Kamiyama K-111-2

by Takayama Instruments Inc.

Kamiyama K-111-2 is a Class I device made by Takayama Instruments Inc., listed in FDA GUDID since 26 Jun 2025 (UDI-DI 04580036672830), 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 Number04580036672830 UDI-DI Date26 Jun 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  • Withdrawn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
Kamiyama
Generic name
General-purpose surgical scissors, reusable
Model / Ref / Catalog
K-111-2
Primary DI / UDI-DI
04580036672830
FDA product code
LRW, GZX
GMDN term
General-purpose surgical scissors, reusable
Device class
Class I
Regulation number
878.4800, 882.4525
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose surgical scissors, reusable

Similar devices in this category

Other devices filed under General-purpose surgical scissors, reusable.

Other devices from Takayama Instruments Inc.

See all devices from Takayama Instruments Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)