18 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Intense pulsed light device, Model(s): DE01A-B, DE01A-G, DE01B-B, DE01B-G, DE01C-B, DE01C-G, DE02A-B, DE02A-G, DE02B-B, DE02B-G, DE02C-B, DE02C-G.
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD BBL™ Sensi-Disc™ Cefoperazone 75 µg
FDA UDI
BECTON, DICKINSON AND COMPANY·30382902316139·BD BBL™ Sensi-Disc™ Cefoperazone 75 µg
Pro-Link Stand-Alone Cervical Spacer System
FDA UDI
Life Spine, Inc.·00190837013677·
Pro-Link Stand-Alone Cervical Spacer System
FDA UDI
Life Spine, Inc.·00190837013660·
Pro-Link Stand-Alone Cervical Spacer System
FDA UDI
Life Spine, Inc.·00190837013691·
Ti Pro-Link Stand-Alone Cervical System
FDA UDI
Life Spine, Inc.·00190837017613·
Ti Pro-Link Stand-Alone Cervical System
FDA UDI
Life Spine, Inc.·00190837017620·
Pro-Link Stand-Alone Cervical Spacer System
FDA UDI
Life Spine, Inc.·00190837013684·
Ti Pro-Link Stand-Alone Cervical System
FDA UDI
Life Spine, Inc.·00190837017637·
Ti Pro-Link Stand-Alone Cervical System
FDA UDI
Life Spine, Inc.·00190837017644·
Freestyle Lancing Device II, Autolet, Autolet Lite, Unilet Lancets
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Stern Fix Sternal Stabilization System
FDA 510(k)
FDA Class 2
·Orthopedic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523151615·Tesera-k SA, 31mm X 26mm X 13mm, 17° Lordosis, T3
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523156689·Tesera-k ALIF, 31W X 26D, 13mm, 17° Trial
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523157433·Tesera-k ALIF, 31W X 26D, 13mm, 17° Broach
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 6, 2014
TRACER METRO DIRECT WIRE GUIDE
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL INC·Product code KOG·August 15, 2011
MANUAL ORTHOPEDIC SURGICAL INSTRUMENT
FDA Adverse Event
Malfunction
·MSD BARTLETT MFG·Product code LXH·July 17, 2013