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Codman® 201038

by Integra LifeSciences Production Corporation

Codman® 201038 (20-1038) is a Class II device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 1 Apr 2020 (UDI-DI 10381780511632), 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 Number10381780511632 UDI-DI Date1 Apr 2020ListedStatusListed 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  • Withdrawn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
Codman®
Generic name
Scalp clip applier, single-use
Model / Ref / Catalog
201038, 20-1038
Primary DI / UDI-DI
10381780511632
FDA product code
HBO
GMDN term
Scalp clip applier, single-use
Device class
Class II
Regulation number
882.4150
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HBO (CLIP, SCALP).

Other devices from Integra LifeSciences Production Corporation

See all devices from Integra LifeSciences Production Corporation →

Properties

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