21 results
·
18ms
·
Sources: EU EUDAMED, US FDA
DUODERM(R) CGF
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Precept
FDA UDI
Nuvasive, Inc.·00887517431516·PRECEPT Screw, 10.5x50mm Fixed
Signature
FDA UDI
SILEX MEDICAL, LLC·B3315881050·Locking Fundus Tri-Max Grasping Forceps
PULSE
FDA UDI
Nuvasive, Inc.·00887517984814·Pulse II Touchsceen Monitor
Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403140990·Snowden-Pencer SENN RETRACTOR SHARP OVERALL LEN...
Signature
FDA UDI
SILEX MEDICAL, LLC·B331588105045·Locking Long Fundus Tri-Max Grasping Forceps
AlligatorTM
FDA UDI
Micro Therapeutics, Inc.·00847536014060·FA-88810-50 ALLIGATOR RETRIEVAL 5MM
Alligator
FDA UDI
Micro Therapeutics, Inc.·00836462014046·Retrieval Device
AlligatorTM
FDA UDI
Micro Therapeutics, Inc.·00847536014039·FA-88810-50 ALLIGATOR DEVICE ARD 5MM
Desio (hioxifilcon D) Daily Wear Soft (hydrophilic) Contact Lenses (Clear and Tinted)
FDA 510(k)
FDA Class 2
·Ophthalmic
PARIETEX PROGRIP MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NexGen®
FDA UDI
Zimmer, Inc.·00889024200227·
NexGen®
FDA UDI
Zimmer, Inc.·00889024200173·
NexGen®
FDA UDI
Zimmer, Inc.·00889024200234·
NexGen®
FDA UDI
Zimmer, Inc.·00889024200180·
NexGen®
FDA UDI
Zimmer, Inc.·00889024200203·
NexGen®
FDA UDI
Zimmer, Inc.·00889024200210·
NexGen®
FDA UDI
Zimmer, Inc.·00889024200197·
POSEY KEEPSAFE DELUXE
FDA Adverse Event
Malfunction
·J. T. POSEY CO.·Product code KMI·April 8, 2014
TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·October 25, 2010