159 results · 19ms · Sources: EU EUDAMED, US FDA

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BresoDX1

FDA 510(k)
FDA Class 2 ·Anesthesiology

EVOS Lumbar Interbody System

FDA UDI
Cutting Edge Spine, LLC·00841193115009·HA PEEK EVOS Straight, ,12mmx8mmx 22mm , BICONV...

PMT® Halo Systems

FDA UDI
PMT CORPORATION·00650551122784·HALO, 1220-5 VEST SMALL, LAMBSWOOL LINER, 1211-...

Zavation

FDA UDI
Zavation LLC·00842166132726·Ti3Z CIF 14mmx16mmx12mm -0 deg

LEONE SPA

FDA UDI
LEONE SPA·08033707022060·CALIBRA BANDS 2ND MOLAR n.SUR 12

KeyLift™

FDA UDI
FLOSPINE LLC·B1830712200120·KeyLift XL 20mm Lg x 12mm H

INTEGRA JARIT VIDEO ASSISTED THORACIC SURGERY INSTRUMENTS

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

MODIFICATION TO RENEGADE FIBER BRAIDED MICROCATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

ZIMMER

FDA Adverse Event
Injury ·ZIMMER·Product code HTG·March 28, 1995

MG PATELLA

FDA Adverse Event
Injury ·ZIMMER·Product code HTG·October 27, 1995

ZIMMER

FDA Adverse Event
Injury ·ZIMMER·Product code HTG·March 4, 1994

ZIMMER

FDA Adverse Event
Injury ·ZIMMER·Product code HTG·January 25, 1995

ZIMMER

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code HTG·October 1, 1996

ZIMMER

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code HTG·August 5, 1997

ZIMMER

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·February 16, 1998

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Aurora EV-ICD System

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 25, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 3, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 19, 2025