16 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SET
FDA 510(k)
FDA Class 2
·Dental
Subtalar MBA Implant System
FDA UDI
Smith & Nephew, Inc.·00885556865996·8MM SIZER
MBA™ Titanium Subtalar Implant System
FDA UDI
Ascension Orthopedics, Inc.·10381780280446·MBA™ Titanium Subtalar Implant System 8MM SIZER...
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193103235·HA PEEK EVOS Curved, , 8mmx9mmx 30mm , FLAT 0 d...
Dissector
FDA UDI
HOTRY (Beijing) Co., Ltd.·06975854250830·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0310080·Probe, 1.5 inch Ball, Lenke, Thoracic, Straight...
LAP DISC HAND ACCESS DEVICE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GCJ·January 16, 2007
ADVANCED ORTHOPAEDIC SOLUTIONS TROCHANTERIC NAIL
FDA 510(k)
FDA Class 2
·Orthopedic
TEMPTELLER INFRARED EAR THERMOMETER, MODELS TT-901, TT-911 AND TT-921
FDA 510(k)
FDA Class 2
·General Hospital
EchoLUTION Viral RNA/DNA Kit (8 x 48)
FDA UDI
BioEcho Life Sciences GmbH·04260759850189·
LEVEL 1® EQUATOR® CONVECTIVE WARMING ACCESSORY
FDA Adverse Event
Injury
·SMITHS MEDICAL ASD; INC.·Product code DWJ·June 12, 2019
LEVEL 1® EQUATOR® CONVECTIVE WARMING DEVICE
FDA Adverse Event
Injury
·SMITHS MEDICAL ASD; INC.·Product code DWJ·June 11, 2019
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 10, 2013
EXT SET 7IN REM CLAVE SITE NDEHP
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPK·April 4, 2011
RIATA ST ACTIVE FIXATION LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
ENDOPATH THORACIC ENDO LINEAR CUTTER W/SAFETY LOCK
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GAG·November 20, 1997