18 results
·
20ms
·
Sources: EU EUDAMED, US FDA
INNER PEACE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ArgenZ HT+ 95x25 C2
FDA UDI
ARGEN CORPORATION, THE·D818122800·Dental porcelain/ceramic restoration kit
Synechiae Spatula
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896103054·Girard Synechiae Spatula Semi-Sharp Tip
BioHorizons
FDA UDI
BIOHORIZONS IMPLANT SYSTEMS, INC·00847236007898·Internal/Single-stage Surgical Kit
Perfect Fit
FDA UDI
DYMEDIX DIAGNOSTICS, INC.·00817377020247·Cadwell ApneaTrak Pediatric Effort Belt Sensor,...
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702379792·Elvarex 1/Thigh High/Slant-Closed Toe/Top Comfo...
VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
SUNTOUCH TOPICAL HEMOSTATIC DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
BECKER ROUND
FDA UDI
The Wells Johnson Company·B458201228000·Cannula, Becker Round, specify length, diameter...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523100934·L Tibial Baseplate Cemented Stemmed Sz 8
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101795·L Tibial Baseplate Cemented Keeled Sz 8
3I T3® TAPERED IMPLANT 4/3 X 11.5MM
FDA Adverse Event
Injury
·BIOMET 3I·Product code DZE·May 20, 2025
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 20, 2025
LIFEPAK(R) 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015
LIFEPAK® 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 21, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 14, 2011
COAGUCHEK XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·August 14, 2008