11 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EMERGE MEDICAL BONE PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OsteoMed
FDA UDI
OSTEOMED LLC·00845694035453·3.5mm x 36mm Locking Screw
Atoll™
FDA UDI
Seaspine Orthopedics Corporation·10889981052737·3.5mm x 36mm Smooth Shaft Poly Screw Assm. The ...
Sochi
FDA UDI
Altus Spine, LLC·00843210166995·Smooth Shaft Polyaxial Screw, 3.5mm x 36mm
K133532
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·February 2, 2021
IBED WIRELESS WITH IBED AWARENESS
FDA 510(k)
FDA Class 2
·General Hospital
MASTERKA 40 MASTERKA 35 MASTERKA 30
FDA 510(k)
FDA Unclassified
·Unknown
HNM LATERAL ANCHOR
FDA Adverse Event
Injury
·HNM STAINLESS, LLC DBA HNM MEDICAL·Product code HWC·April 16, 2018
PASSIVE PLANAR BLUNT PROBE
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·October 1, 2014
GYNECARE GYNEMESH* PS
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTO·May 29, 2013
NEXGEN MIS STEMMED TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·June 15, 2011