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Cortical Tap 8140-99-472

by Biomet Orthopedics, Inc.

Cortical Tap 8140-99-472 (814099472) is a Class I device made by Biomet Orthopedics, Inc., listed in FDA GUDID since 28 Jul 2017 (UDI-DI 00887868036521), 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 Number00887868036521 UDI-DI Date28 Jul 2017ListedStatusListed 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  • Withdrawn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
Cortical Tap
Generic name
Bone tap, reusable
Model / Ref / Catalog
8140-99-472, 814099472
Primary DI / UDI-DI
00887868036521
FDA product code
HWX
GMDN term
Bone tap, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone tap, reusable

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Other devices filed under Bone tap, reusable.

Other devices from Biomet Orthopedics, Inc.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)