53 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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uMR570
FDA 510(k)
FDA Class 2
·Radiology
EarQ
FDA UDI
Oticon A/S·05707131350428·G50 S, BTE PP 13 2.4G 105 C094 EARQ
16PW - Loggers - Poly White
FDA UDI
Certified Safety Manufacturing, Inc.·00766588015040·16PW - Loggers - Poly White
Symmetry Olsen
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00841785105388·
Ti-one 101
FDA UDI
HUNG CHUN BIO-S CO., LTD.·04719871590287·Abutment Ø4.5, 4 mm Abt. H
The Ti-one 101 Denta...
ABSORBENT PAPER POINTS
FDA UDI
DiaDent Group International·08806383512251·"An absorbent paper points is an endodontic pap...
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78820154000201·EXP MBT 018/U4 UNIV -7T 0A
RUSCH EDGAR TUBE
FDA 510(k)
FDA Class 2
·Anesthesiology
GRANITEC DUAL-CURE CORE BUILD-UP, N'DURANCE DIMER CORE
FDA 510(k)
FDA Class 2
·Dental
BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code QJR·August 5, 2020
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 10, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 10, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 10, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 10, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 10, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 10, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 10, 2016
GORE PROPATEN VASCULAR GRAFT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DSY·October 17, 2008
ENRHYTHM DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code DXY·August 11, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 2, 2013