14 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
HBOTC Muscle and Nerve Stimulator
FDA 510(k)
FDA Class 2
·Neurology
Denovo general purpose dental molar band
FDA UDI
Denovo Dental, Inc.·00810059290488·Denovo general purpose dental molar band - Mand...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197059619·Jobson-Horne aural probe
140mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197059626·Jobson-Horne aural probe
180mm,...
SOUND SURGICAL TECHNOLOGIES LLC POWERX LIPO SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
E SURGICAL ELECTROSURGICAL PATIENT RETURN ELECTRODE, DUAL PLATE WITH CORD AND ELECTROSURGICAL PATIENT RETURN ELECTRODE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·May 15, 2023
GORE DRYSEAL FLEX INTRODUCER SHEATH
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DYB·October 19, 2020
GORE® DRYSEAL FLEX INTRODUCER SHEATH
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DYB·October 6, 2016
ASR ACETABULAR CUPS 54
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·June 10, 2013
PVC, CLEAR, CONTRAST INJECTION TUBING
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code DXJ·June 2, 2011
COLLEAGUE VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008
GORE® DRYSEAL FLEX INTRODUCER SHEATH
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DYB·May 30, 2023
QUADRA-H CEMENTLESS, HA COATED STEM SIZE 6 STD, SHORT NECK
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·February 24, 2017