577 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PhoeniX
FDA 510(k)
FDA Class 2
·Radiology
Bernafon
FDA UDI
Bernafon AG·05711584086858·ZR3, KIT 312 NFM 85 PB L BE ZERENA 3
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304463196·
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260421·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694019064·2.0mm x 11mm Cannulated Lag Screw
9.2MHZ PENCIL PROBE
FDA UDI
PARKS MEDICAL ELECTRONICS, INC.·00816787021462·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070140·Cannulated 2.0 x 11mm Lag Screw Sterile Qty 5
NORM SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ECLIPSE TREATMENT PLANNING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
G7 NEUTRAL E1 LINER 32MM F
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code PBI·July 24, 2017
32MM MOD HEAD COCR STD NECK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·July 24, 2017
5FR DUAL-LUMEN UVC CATH
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FOS·September 12, 2011
OPTI-FREE REPLENISH
FDA Adverse Event
Injury
·ALCON - FORT WORTH / ALCON LABORATORIES, INC.·Product code LPN·June 16, 2011
UNKNOWN DEPUY INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·October 6, 2008
NEXGEN CR-FLEX FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·June 20, 2013
HILL-ROM 405 ELECTRIC BED
FDA Adverse Event
Malfunction
·HILL-ROM DE MEXICO S DE RL DE CV·Product code FNL·July 29, 2011
O.B. UNSPECIFIED
FDA Adverse Event
Malfunction
·MONTREAL SAN PRO·Product code HEB·April 19, 2011
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS - HOUSTON·Product code MUZ·October 10, 2019
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code HQL·January 26, 2012
TENDRIL SDX
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code NVZ·August 12, 2023