22 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STGC
FDA 510(k)
FDA Class 2
·Orthopedic
K121116
FDA UDI
Life Spine, Inc.·00190837016029·
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837016043·
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837016258·
CHS
FDA UDI
Smith & Nephew, Inc.·03596010062499·COMPRESSION HIP SCREW LAG SCREW 130MM
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780377344·Integra® Jarit® Ryder Needle Holder, 7-3/4", Ca...
E.M Adams co, inc.
FDA UDI
E.M. ADAMS, INC.·50840200301409·ABDOMINAL BINDER
E.M Adams co, inc.
FDA UDI
E.M. ADAMS, INC.·58100013401409·ABDOMINAL BINDER
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450572900·
COMPUMEDICS SOMTE SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
OSTEOMED LOW PROFILE NEURO FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
HISTOACRYL FLEXIBLE PACK 5
FDA Adverse Event
Injury
·B.BRAUN SURGICAL SA·Product code MPN·July 23, 2019
VERTECEM V+ CEMENT KIT
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code NDN·March 28, 2013
VERTECEM V+ CEMENT KIT
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code NDN·February 27, 2013
VERTECEM V+ CEMENT KIT
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code NDN·March 1, 2013
VERTECEM V+ CEMENT KIT
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code NDN·February 27, 2013
ARTOURA BREAST TISSUE EXPANDER
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code LCJ·March 31, 2020
RESERVOIR 1.8ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·May 20, 2013
DELTA CER HEAD 12/14 36MM +1.5
FDA Adverse Event
Injury
·DEPUY IRELAND 9616671·Product code LZO·September 26, 2014
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 13, 2011