857 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SmoothSkin BARE+
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304463103·
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260414·
Bernafon
FDA UDI
Bernafon AG·05711584086841·ZR3, KIT 312 NFM 85 PB R BE ZERENA 3
Ceramco® II Silver™
FDA UDI
Dentsply International Inc.·D0011920100·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694009584·2.0mm x 10mm Cannulated Lag Screw
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101087·HELVESTON "BARBIE" RETRACTOR
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001131920100·Trial-OneLIF Interbody, Large, 19 Degree, 20mm ...
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K1220100·Breaker, Extended Tab
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001031920100·OneLIF Interbody, Large, 19 Degree, 20mm X 10mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070126·Cannulated 2.0 x 10mm Lag Screw Sterile Qty 5
VACUETTE PREMIUM SAFETY BLOOD COLLECTION SET
FDA 510(k)
FDA Class 2
·General Hospital
PC ECG, MODEL SE-1010
FDA 510(k)
FDA Class 2
·Cardiovascular
OPTI-FREE REPLENISH
FDA Adverse Event
Injury
·ALCON - FORT WORTH / ALCON LABS, INC.·Product code LPN·July 28, 2010
ACRYSOF IQ TORIC
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·July 23, 2010
NEXGEN MIS STEMMED TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·September 29, 2011
NEXGEN STEMMED TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·June 20, 2013
PINNACLE MTL INS NEUT36IDX52OD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD·Product code KWA·October 6, 2008
TAXUS (R) LIBERTÉ (R)
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·August 4, 2011
AUTO SUTURE
FDA Adverse Event
Malfunction
·Product code GDW·February 19, 2010