31 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HammerFiX Device
FDA 510(k)
FDA Class 2
·Orthopedic
Inspire™ Esthetic Provisional Composite A2 Kit
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172010764·Crown and Bridge Temporary Resin
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704508833·
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184200·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184224·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184118·Femoral segment, cemented, UHMWPE, Ti6Al4V, for...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184132·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184231·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184248·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184163·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184194·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184156·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184125·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184149·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
LINK Endo-Model EVO Knee System
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575184217·Femoral segment, uncemented, CoCrMo, Ti6Al4V, L...
NEO-SERVO I
FDA 510(k)
FDA Class 2
·General Hospital
VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,
FDA 510(k)
FDA Class 2
·Dental
RADIFOCUS GLIDEWIRE M
FDA Adverse Event
Injury
·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 22, 2018
TRULIANT TIB IMP PSC INSERT SZ 6, 15MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·September 11, 2024
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 8, 2014