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Ezloc™ 904779

by Biomet Orthopedics, Inc.

Ezloc™ 904779 is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K053461 on 3 Feb 2006 and listed in FDA GUDID since 28 Jul 2017 (UDI-DI 00880304992269), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K053461

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00880304992269 UDI-DI Date28 Jul 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK053461 Date3 Feb 2006DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K053461 decided 3 Feb 2006 Active
  • FDA GUDID UDI-DI 00880304992269 listed 28 Jul 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K053461
  2. Listed FDA GUDID 00880304992269

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Ezloc™
Generic name
Ligament bone anchor
Model / Ref / Catalog
904779
Primary DI / UDI-DI
00880304992269
510(k) Number
FDA product code
MBI, HWC
GMDN term
Ligament bone anchor
Device class
Class II
Regulation number
888.3040
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ligament bone anchor

Cleared under the same submission (K053461)

and 1 more cleared under K053461

Similar devices in this category

Other devices filed under Ligament bone anchor.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)