Skip to content

Ambler Surgical Cobb spinal fusion curette

by Ambler Surgical, LLC 39 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Overview

Ambler Surgical's Cobb spinal fusion curette is a high-quality, manual surgical instrument designed for cutting and excising bone tissue during orthopaedic or plastic surgery procedures. This reusable device features a reverse angled handle with a sharp edge at the distal end, made of high-grade stainless steel for durability and precision.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00190660021108 UDI-DI Date4 Jan 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Ambler Surgical
Generic Name
Bone curette, reusable
Model / Ref / Catalog
Cobb spinal fusion curette, 19-955
Primary DI / UDI-DI
00190660021108
FDA Product Code
HAO
GMDN Term
Bone curette, reusable
Device Class
Class I
Regulation Number
882.4535
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Bone curette, reusable

Other devices from Ambler Surgical, LLC

See all devices from Ambler Surgical, LLC →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No