Home › Biomet Orthopedics, LLC › REGENEREX RINGLOC + HIP SYSTEM

REGENEREX RINGLOC + HIP SYSTEM

Biomet Orthopedics, LLC · Model PT-104048 · UDI-DI 00880304455191

MAY LWJ JDG LZO LPH KWZ MEH JDI MBL Prescription

510(k) clearances

499

Adverse events

Recalls

Facilities

Recalls

Date	Firm	Reason
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
2016-01-21	Stryker Howmedica Osteonics Corp.	During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.