46 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DISKOM
FDA 510(k)
FDA Class 2
·Orthopedic
BI-METRIC X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304182646·
BI-METRIC X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304182943·
BI-METRIC X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304182349·
Tibial Trial Tray
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215062064·
Orthopedic Instruments
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258699639·
12 LEAD GLOVE
FDA 510(k)
FDA Class 2
·Cardiovascular
DERMA SCIENCES MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEY
FDA 510(k)
FDA Unclassified
·Unknown
REAMER SHAFT, MOD. TRINKLE BIXCUT 8.0 X 284 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·December 18, 2012
COCR CABLE/SLEEVE SET 2.0MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDQ·December 13, 2017
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 17, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·June 20, 2013
32MM M2A MOD HEAD STD NK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 16, 2020
M2A-TAPER LINER SZ 41/32
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 16, 2020
M2A-T UNIV 2-HOLE SHL SZ 41/58
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 16, 2020
M2A-MAGNUM PF CUP 58OD/52ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·January 19, 2018
M2A-MAGNUM MOD HD SZ 52MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·January 19, 2018
BI-METRIC/X POR NC 15X155
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MEH·September 27, 2017
PRODIGY AUTOCODE
FDA Adverse Event
Injury
·OK BIOTECH CO., LTD.·Product code NBW·April 12, 2019