159 results
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19ms
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Sources: EU EUDAMED, US FDA
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