65 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARIX Humerus System
FDA 510(k)
FDA Class 2
·Orthopedic
BRUSIO 2.5mm Flex Straight Plate, 8 Hole
FDA UDI
Bonebridge AG·07640187463231·
External Fixation
FDA UDI
Life Spine, Inc.·00190837023249·60mm Threaded Rod
Ophthalmic Ring
FDA UDI
KATENA PRODUCTS, INC.·00841668100813·FLIERINGA FIXATION RING 20MM
Arena-C®
FDA UDI
SPINEFRONTIER, INC.·00190361021148·12x15 Arena-C HA PEEK Lordotic 12mm
Arena-C®
FDA UDI
SPINEFRONTIER, INC.·00190361021087·12x15 Arena-C HA PEEK Lordotic 6mm
Arena-C®
FDA UDI
SPINEFRONTIER, INC.·00190361021094·12x15 Arena-C HA PEEK Lordotic 7mm
Arena-C®
FDA UDI
SPINEFRONTIER, INC.·00190361021117·12x15 Arena-C HA PEEK Lordotic 9mm
Arena-C®
FDA UDI
SPINEFRONTIER, INC.·00190361021124·12x15 Arena-C HA PEEK Lordotic 10mm
Arena-C®
FDA UDI
SPINEFRONTIER, INC.·00190361021070·12x15 Arena-C HA PEEK Lordotic 5mm
Arena-C®
FDA UDI
SPINEFRONTIER, INC.·00190361021131·12x15 Arena-C HA PEEK Lordotic 11mm
Arena-C®
FDA UDI
SPINEFRONTIER, INC.·00190361021100·12x15 Arena-C HA PEEK Lordotic 8mm
GLIDESHEATH
FDA 510(k)
FDA Class 2
·Cardiovascular
BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER
FDA 510(k)
FDA Class 2
·Cardiovascular
SANTORINI™ Corpectomy Cage System
FDA UDI
VB Spine LLC·10888857243095·Cage Inserter, Size 12x17 mm
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·September 18, 2008
DEPUY ASR XL FEM IMP SIZE 41
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·October 2, 2014