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ToggleLoc 904722

by Biomet Orthopedics, Inc.

ToggleLoc 904722 is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K130033 on 1 Aug 2013 (3 earlier submissions) and listed in FDA GUDID since 24 Oct 2015 (UDI-DI 00880304453289), active as of 23 Oct 2026. 9 FDA recalls are linked to it.

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

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 ongoing

This device is named in the recall

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00880304453289 UDI-DI Date24 Oct 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK130033 Date1 Aug 2013DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K130033 decided 1 Aug 2013 Active· +3 more in the status table
  • FDA GUDID UDI-DI 00880304453289 listed 24 Oct 2015 Listed

Recalls

9 recalls · 1 ongoing · FDA

    • Ongoing Z-0212-2026 FDA Class II initiated 23 Sep 2025

    There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop

    • Terminated Z-0818-2018 FDA Class II initiated 22 Aug 2017

    Ziptight Ankle Syndesmosis Fixation was packaged without the tip protectors.

    • Terminated Z-1828-2016 FDA Class II initiated 1 Apr 2016

    Insufficient seal strength on sterile barrier packaging. The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile. If the product becomes non-sterile and is used or implanted, it may lead to an infection.

    • Terminated Z-1363-2015 FDA Class II initiated 26 Feb 2015

    The firm is recalling ToggleLocs and Ziploops manufactured in May and July of 2014 as they were not processed following a standard work process, which resulted in complaints of sterile packaging not being sealed.

  • 2 recalls, same reason

    • Terminated Z-1953-2010 FDA Unclassified (pre-2012) initiated 31 Mar 2010
    • Terminated Z-1952-2010 FDA Unclassified (pre-2012) initiated 31 Mar 2010

    The firm has received complaints that the saddle is too long. The saddle is supposed to be between 7/8 and 1 1/8 inches long. The saddle in the complaints was up to 1.9 inches long.

  • 2 recalls, same reason

    • Terminated Z-0560-2010 FDA Unclassified (pre-2012) initiated 10 Nov 2009
    • Terminated Z-0559-2010 FDA Unclassified (pre-2012) initiated 10 Nov 2009

    Packages labeled as containing a stainless steel device actually contain a titanium device, and vice versa.

    • Terminated Z-0582-2012 FDA Unclassified (pre-2012) initiated 24 Apr 2008

    Six sizes of ToggleLoc, Artificial Ligament Fixation Device, have been manufactured with the suture pull hole drilled in the wrong location on the device. The ToggleLoc implant is deployed with a suture that pulls the device through the tunnel. The hole being drilled in the wrong location will orient the device to pass through the tunnel with the angled end of the implant first. This may caus

Timeline

14 dated events

  1. Recall initiated FDA recalls Z-0560-2010
  2. Recall initiated FDA recalls Z-0559-2010
  3. Recall initiated FDA recalls Z-1953-2010
  4. Recall initiated FDA recalls Z-1952-2010
  5. Cleared FDA 510(k) K130033
  6. Recall initiated FDA recalls Z-1363-2015
  7. Listed FDA GUDID 00880304453289
  8. Recall initiated FDA recalls Z-1828-2016
  9. Recall initiated FDA recalls Z-0818-2018
  10. Recall initiated FDA recalls Z-0212-2026

4 earlier events are in the sections above.

Coverage

1 jurisdiction

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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
ToggleLoc
Generic name
Tendon/ligament bone anchor, non-bioabsorbable
Model / Ref / Catalog
904722
Primary DI / UDI-DI
00880304453289
510(k) Number
FDA product code
JDR, MBI
GMDN term
Tendon/ligament bone anchor, non-bioabsorbable
Device class
Class II
Regulation number
888.3030, 888.3040
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Tendon/ligament bone anchor, non-bioabsorbable

Cleared under the same submission (K033838)

and 7 more cleared under K033838

Cleared under the same submission (K083070)

and 8 more cleared under K083070

Similar devices in this category

Other devices filed under Tendon/ligament bone anchor, non-bioabsorbable.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)