16 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OMNICUT RESECTION BLADE
FDA 510(k)
FDA Class 2
·Orthopedic
A.S.A.P.® All Surface Access Polishers 6-Pack Refill (Large)
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172012898·Dental polishing point
A.S.A.P.® All Surface Access Polishers 6-Pack Refill (Large)
FDA UDI
DEN-MAT HOLDINGS, LLC·00359883003067·Dental polishing point
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037313213·STABILITY TRIAL HUMERAL CUP 135/145° Ø36 +12
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321309120·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311309120·
Humeral Cup Stability
FDA UDI
FX SOLUTIONS·03701037314081·STABILITY TRIAL HUMERAL CUP CUSTOM MADE 135/145...
Scorpio
FDA UDI
Howmedica Osteonics Corp.·07613154006038·Posterior Stabilized Tibial Insert
THYRO TEST
FDA 510(k)
FDA Class 2
·Clinical Chemistry
DISPOSABLE NERVE STIMULATING PROBE, BIPOLAR CONCENTRIC, DISPOSABLE NERVE STIMULATOR PROBE, BIPOLAR SIDE BY SIDE
FDA 510(k)
FDA Class 2
·Neurology
SCORPIO TOTAL KNEE PS; TIBIAL BEARING INSERT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·June 29, 2016
COULTER® LH 780 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·May 24, 2013
TECNIS 1-PIECE
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL OPTICS·Product code HQL·June 16, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·August 21, 2008
RESPIRATORY HUMIDIFIER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·June 16, 2014
VENTED AUTOFEED CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·April 3, 2014