11 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Caphosol® Artifical Saliva (32 doses sachet box)
FDA 510(k)
FDA Unclassified
·Unknown
Manta Ray™
FDA UDI
Seaspine Orthopedics Corporation·10889981057527·Screw - Self-Tapping - Variable - 4.0x15 mm
Inter-Lock
FDA UDI
STRYKER CORPORATION·04546540392237·INTER-LOCK CROSS PIN PLLA - 50MM
Insignia
FDA UDI
ALPHATEC SPINE, INC.·00190376266626·4.0mm Fixed Angle, Self Tapping Screw, Dual Lea...
Inter-Lock
FDA UDI
STRYKER CORPORATION·04546540392220·INTER-LOCK CROSS PIN PLLA PACKAGING 35MM
M-PM-DISC
FDA 510(k)
FDA Unclassified
·Unknown
EARLOOP PROCEDURE MASK
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STYLE 68 SALINE FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FWM·May 13, 2025
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 7, 2014
LOCKING SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code NKB·August 31, 2011
ENTERPRISE 9000
FDA Adverse Event
Malfunction
·ARJOHUNTLEIGH POLSKA SP. ZO.O.·Product code FNL·July 11, 2013