716 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SOLAX
FDA 510(k)
FDA Class 2
·Physical Medicine
CoRoent
FDA UDI
Nuvasive, Inc.·00887517636942·CoRoent Ant TLIF PEEK, 13x11x30mm 12°
COE-FLEX®
FDA UDI
Gc America Inc.·10386040004923·COE-FLEX® s Regular Body (catalyst only) (1 x 4...
COE-FLEX®
FDA UDI
Gc America Inc.·D6581313021·COE-FLEX® s Regular Body (catalyst only) (1 x 4...
CHESAPEAKE Stabilization System
FDA UDI
VB Spine LLC·10888857560062·Universal Driver Size 20
SUSTAIN SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
ALEUTIAN IBF SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123148·19mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123162·21mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123124·17mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123100·15mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123063·11mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123070·12mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123131·18mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123155·20mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123094·14mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123117·16mm Broach, 30 x 26, 12° Lordosis
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523123087·13mm Broach, 30 x 26, 12° Lordosis
VITROS IMMUNODIAGNOSTICS PRODUCTS TROPI ES REAGENT PACK
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·October 1, 2014
PROTAPER UNIVERSAL ROTARY FILE
FDA Adverse Event
Injury
·DENTSPLY MAILLEFER·Product code EKS·May 15, 2013