Codman® 201039
by Integra LifeSciences Production Corporation 2 variants
Codman® 201039 (20-1039) is a Class II device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 28 Feb 2020 (UDI-DI 10381780511649), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10381780511649 | Date28 Feb 2020 | StatusListed |
Official records
- AccessGUDID record 10381780511649
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Codman®
- Generic name
- Scalp clip forceps
- Model / Ref / Catalog
- 201039, 20-1039
- Primary DI / UDI-DI
- 10381780511649
- FDA product code
- HBO
- GMDN term
- Scalp clip forceps
- Device class
- Class II
- Regulation number
- 882.4150
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code HBO (CLIP, SCALP).
- RANEY AND LEROY-RANEY SCALP CLIP by New England Surgical Instrument Corp.
- Medtronic Clip Gun Kit by Medtronic Neurosurgery
- Clip Gun with Raney Type Scalp Clips by Omni Medical Designs
- Codman RF-12 Disposable Scalp Clip Applier by Codman & Shurtleff, Inc.
- SCALPFIX CLIP SYSTEM by AESCULAP, INC.
- CODMAN DISPOSABLE SCALP CLIP APPLIER by Codman & Shurtleff, Inc.
- STORZ RANEY SCALP CLIP, MODEL 1-20-004-05 by Rudolf Storz GmbH
- RANEY CLIPS by Zimmer, Inc.
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