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Taperloc Complete Microplasty 51-208240

by Biomet Orthopedics, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

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

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00880304747777 UDI-DI Date28 Jul 2017ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Taperloc Complete Microplasty
Generic Name
Bone file/rasp, manual, reusable
Model / Ref / Catalog
51-208240
Primary DI / UDI-DI
00880304747777
510(k) Number
FDA Product Code
KWY, LPH, KWL, MEH, JDI, LZO, OQG, KWZ
GMDN Term
Bone file/rasp, manual, reusable
Device Class
Class II
Regulation Number
888.3390, 888.3358, 888.3360, 888.3353, 888.3350, 888.3310
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Bone file/rasp, manual, reusable

Cleared under the same submission (K110400)

Show all (12)

Other devices from Biomet Orthopedics, Inc.

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Properties

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

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
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No