8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Extension Set
FDA 510(k)
FDA Class 2
·General Hospital
ENCOMPASS 10*17 AND 12*17 EXTENDED PRESS-FIT HIP STEMS
FDA 510(k)
FDA Class 2
·Orthopedic
PASTELLE Q-SWITCHED ND: YAG LASER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·June 8, 2013
ZIMMER M/L TAPER HIP FEMORAL STEM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code LPH·June 30, 2011
DURALOC CONST LINER 48X28
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·September 4, 2008
MYSPINE UNILATERAL LEFT GUIDE S01
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code PQC·August 22, 2024
ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear
FDA Enforcement
Class II
·Ongoing·Elekta, Inc.·December 13, 2023