Home › INTEGRA LIFESCIENCES PRODUCTION CORPORATION › Integra® Miltex®
Integra® Miltex®
INTEGRA LIFESCIENCES PRODUCTION CORPORATION · Model 013-31210 · UDI-DI 10381780505976
EHZ
Prescription
10
510(k) clearances
9
Adverse events
1
Recalls
141
Facilities
Description
Pulp Canal Aspirator Tip, Large
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-11-02 | Stradis Medical, LLC dba Stradis Healthcare | Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in |
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 keyRead the docsData 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.