117 results
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37ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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PressureWire X
FDA 510(k)
FDA Class 2
·Cardiovascular
Comprehensive® Reverse Shoulder
FDA UDI
Biomet Orthopedics, LLC·00880304555396·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197083645·FINOCHIETTO TC Needle holder
20 cm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197083652·FINOCHIETTO TC Needle holder
27 cm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197385626·PAR TC Needle holder, delicate
135mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197385619·PAR TC Needle holder, delicate
12cm, ...
QUANTA DIODE LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STERITITE CONTAINER SYSTEM & MEDITRAY PRODUCTS
FDA 510(k)
FDA Class 2
·General Hospital
QUANTA SYSTEM S.P.A.
FDA Adverse Event
Malfunction
·QUANTA SYSTEM, S.P.A.·Product code GEX·December 21, 2012
COMP RVS CNTRL SCR 6.5X30MM ST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·August 30, 2018
COMP RVRS SHLDR GLNSP STD 36MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·August 29, 2018
ARCOM XL 44-36 STD HMRL BRNG
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·August 29, 2018
COMP RVRS 25MM BSPLT HA+ADPTR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PHX·July 18, 2023
PLM A+ CANADIAN VII
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·October 15, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 20, 2013
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code MGB·July 27, 2011
COMPREHENSIVE REVERSE GLENOSPHERE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PAO·August 6, 2018
COMP RVRS 25MM BSPLT HA+ADPTR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·January 26, 2026
COMP NLK SCR 3.5HEX 4.75X15 ST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·November 26, 2019
COMP LK SCR 3.5HEX 4.75X20 ST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·November 26, 2019