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Centurion 67935

by Centurion Medical Products

Centurion 67935 is a Class I device made by Centurion Medical Products, listed in FDA GUDID since 1 Jan 2022 (UDI-DI 00653160208986), 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 Number00653160208986 UDI-DI Date1 Jan 2022ListedStatusListed 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  • Withdrawn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
Centurion
Generic name
General-purpose surgical scissors, single-use
Model / Ref / Catalog
67935
Primary DI / UDI-DI
00653160208986
FDA product code
LRW
GMDN term
General-purpose surgical scissors, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose surgical scissors, single-use

Similar devices

Other devices filed under FDA product code LRW (SCISSORS, GENERAL, SURGICAL).

Other devices from Centurion Medical Products

See all devices from Centurion Medical Products →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)