35 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ExcelsiusGPS Spine 1.1 Interbody Module
FDA 510(k)
FDA Class 2
·Neurology
Novo Surgical
FDA UDI
NOVO SURGICAL, INC.·00842331122323·Bipolar Instrument Cable, reusable, 12 feet
LEONE SPA
FDA UDI
LEONE SPA·08033707069492·STOP/SURGICAL HOOK CRIMPING PLIERS
Best Medical International
FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365108495·
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122209·KWire .045x4" (1.1x100mm)
Paxeon Remedy
FDA UDI
PAXEON RECONSTRUCTION LLC·08177570201181·Remedy Stem Size 11 Standard Offset
Remedy Hip Stem
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215053192·
Remedy
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215008062·
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161111911000·Orion Stem, Size 11
CROSSFT OC SUTURE ANCHOR MODE CFC-4502, CFC-5502, CFC-6502, CFC-4503, CFC-5503, CFC-6503
FDA 510(k)
FDA Class 2
·Orthopedic
MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
TriVerse Impactor
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215098285·
SKYLON Stem
FDA UDI
AMPLITUDE SAS·03701089520423·
Truliant
FDA UDI
Exactech, Inc.·10885862523594·TRUL FEM IMPACTOR HEAD NON-LOCKING
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·November 20, 2021
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 29, 2021
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 20, 2021
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 29, 2021
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 29, 2021
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 29, 2021