12 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ASAHI CHIKAI V PERIPHERAL VASCULAR GUIDE WIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
ScrewPlant® Implant
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307105244·3.7mmD x 16mmL, 3.7mmD Platform
N/A
FDA UDI
HANS RUDOLPH, INC.·00874750004508·MED QUEST MASK/HG BLUE SWIVEL
GLOBAL ADVANTAGE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295007210·GLOBAL ADVANTAGE POROCOAT STANDARD STEM SIZE 16...
GLOBAL ADVANTAGE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295007203·GLOBAL ADVANTAGE STANDARD STEM SIZE 16 160mm
ROCHE ELECSYS FOLATE RBC; ROCHE ELECSYS FOLATE RBC CALSET
FDA 510(k)
FDA Class 2
·Clinical Chemistry
EVERYWAY LOW BACK PAIN RELIEF SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
GMK EFFICIENCY THREADED PIN Ø3.2 L70 HA3.5 MECHE TRIANGLE
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code LXH·December 13, 2021
BIOFINITY
FDA Adverse Event
Injury
·COOPERVISION MANUFACTURING, LTD.·Product code LPM·May 10, 2013
SUTURE UNKNOWN
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAP·September 24, 2014
OCTRODE LEAD, 60CM LENGTH
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 2, 2011
INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·July 21, 2021