53 results · 32ms · Sources: EU EUDAMED, 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