10 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEONICS OMNIFIT HA HIP STEM SERIES, OSTEONICS SECUR-FIT HA HIP STEM SERIES, OSTEONICS PRIMARY SECUR-FIT PLUS HIP STEMS
FDA 510(k)
FDA Class 2
·Orthopedic
PROPELLER HEAD
FDA UDI
Biomet Orthopedics, LLC·00880304416840·
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091982032·posteriors; shade A4; size XL; upper jaw
Sklar
FDA UDI
SKLAR CORPORATION·10649111376191·MICRO MOSQ FCP STR SERR 4 3/4 IN
Trinias
FDA UDI
SHIMADZU CORPORATION·04540217057917·
SEQUOIA SPINAL SYSTEM (MODEL 3306), SPEEDLINK TRANSVERSE CONNECTOR (MODELS 3308, 3309, 3310)
FDA 510(k)
FDA Class 2
·Orthopedic
SterilContainer S System
FDA 510(k)
FDA Class 2
·General Hospital
ASR ACETABULAR CUPS 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 28, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 5, 2014
UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code LFX·February 8, 2011