14 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
THERAVIEW
FDA 510(k)
FDA Class 2
·Radiology
P.F.C. SIGMA
FDA UDI
DEPUY (IRELAND)·10603295232964·P.F.C. SIGMA TIBIAL INSERT FIXED BEARING TC3 2 ...
ELMED
FDA UDI
ELMED INCORPORATED·00842180172616·OBWEGESER RETRACTOR, 31 X 10MM, 22CM OVERALL LE...
Vibralung Patient Kit with Circulair II Model 0295
FDA UDI
WESTMED, INC.·00709078001505·
Eye Shield
FDA UDI
KATENA PRODUCTS, INC.·00841668111130·EYE SHIELD W/ GARTER ASSORTED PACK OF 50
Life Instruments
FDA UDI
Life Instrument Corporation·M930796051010·Nasal Suction Tube 10FR 120mm working length
ENDOCLAMP AORTIC CATHETER
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code DXC·June 23, 2006
DREW SCIENTIFIC GLYCATED HEMOGLOBIN FIVE LEVEL LINEARITY KIT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
MAKO 7
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
2520274-2013-10228
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code MNI·February 11, 2013
MALLORY/HEAD PRESS FIT FEMORAL 7X140MM STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·January 13, 2011
UNKNOWN DEPUY SLEEVE
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 28, 2014
Depuy P.F.C. E knee system, TC3 tibial insert; polyethylene tibial insert, Sz 2, 10.0 mm; Ref 96-0510.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005
XP-CR Tibial Tray - Interlok 91 mm Item # 195279
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·September 18, 2019