50 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FRACTIONAL SKIN RESURFACING (FSR) APPLICATOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Aequalis™ Adjustable Reversed
FDA UDI
TORNIER, INC.·00846832068135·
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094069860·Welch Allyn PCH-100 Holter Office Software; Hol...
Hallux Osteotomy Plate
FDA UDI
I.T.S. GmbH·09120047298749·Hallux Osteotomy Plate, 10mm
MICROSAFE®
FDA UDI
SAFE-TEC CLINICAL PRODUCTS LLC·05060586450069·
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383501354·Gutta Percha Points is used to root canal filin...
WILLIAMS EYE SPECULUM
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896011984·WILLIAMS EYE SPECULUM WITH LOCKING SCREW LARGE ...
Life Instruments
FDA UDI
Life Instrument Corporation·M93071015100S0·Down Pushing Curette (7" handle)
Life Instruments
FDA UDI
Life Instrument Corporation·M930710151000·Charnley Curette Small 14mmx25mm
Life Instruments
FDA UDI
Life Instrument Corporation·M93071015100C0·Down Pushing Curette 30 deg angle
OS-2000 OPTICAL SONOGRAPHY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
MULTI HI-FLO PNEU, WISAP #7080
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code MUM·October 17, 2017
EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code MUM·December 28, 2017
EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code MUM·October 12, 2017
EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code MUM·August 9, 2017
EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code MUM·July 18, 2017
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 29, 2025
EVOLUTION® DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code MUM·July 18, 2017
900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 2, 2013