100 results
·
30ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Portable Electro-Stimulation Therapy Device
FDA 510(k)
FDA Class 2
·Physical Medicine
PROPELLER HEAD SCREW SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304269170·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1820200·18mm H x 20mm W x 20mm L x 0 degrees XLIF
OsteoMed
FDA UDI
OSTEOMED LLC·00842528127186·2.0 X 20mm Cannulated Headed Screw, T7
FX V 135 stem
FDA UDI
FX SOLUTIONS·03701037318492·FX V135 LONG STEM TA6V CEMENTLESS Ø36/10 LG200m...
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100950·DESMARRES LID RETRACTOR #0
Best Medical International
FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365108310·
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L182020120·18mm H x 20mm W x 20mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X182020120·18mm H x 20mm H x 20mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X18202080·18mm H x 20mm W x 20mm L x 8 degrees XLIF
Origin Trial Neck
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215039790·
Trial Head
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215038335·
mambo™ modular cervical plate system
FDA UDI
Ulrich GmbH & Co. KG·04052536008100·mambo single plate XXS yellow, length 20 mm
DynaClip
FDA UDI
Medshape, Inc.·M9703000001820200·DYNACLIP STAPLE, 18X20X20MM
ENVISION BLOOD GLUCOSE TEST SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
VEGA SPAN SPINOUS PROCESS PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PIPELINE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·December 9, 2020
TITAN
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code FHW·December 9, 2020
MINICAP TRANSFER SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 21, 2013
3002 SECURE II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·June 22, 2011