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6.0mm Disposable Cannulated Flexible Drill CFR-060-LP

by Curvafix Inc GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10850070500002 UDI-DIDate23 Oct 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
6.0mm Disposable Cannulated Flexible Drill
Generic Name
Cannulated surgical drill bit, single-use
Model / Ref / Catalog
CFR-060-LP
Primary DI / UDI-DI
10850070500002
FDA Product Code
HTW
GMDN Term
Cannulated surgical drill bit, single-use
Device Class
Class I
Regulation Number
888.4540
GUDID distribution status
In Commercial Distribution

Other devices from Curvafix Inc

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

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