27 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BORRELIA BURGDORFERI IGG BLOT TEST
FDA 510(k)
FDA Class 2
·Microbiology
SCREW SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304213982·
2870 3WAY SLIDE VALVE
FDA UDI
HANS RUDOLPH, INC.·00817136021959·2870/CLRA/2700 1.375 CP NO SMP
CapSure® Spine System
FDA UDI
Spine Wave, Inc.·10840642105360·PS3 Screw 8.5mm x 45mm
SMR SHOULDER SYSTEM - CTA HUMERAL HEADS
FDA 510(k)
FDA Class 2
·Orthopedic
ANESTHESIA INJECTION TOOL SET
FDA 510(k)
FDA Class 2
·Dental
UNIV RNGLC SHL 60MM/L23
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 3, 2020
UNKNOWN STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·November 3, 2020
RNGLC +5MM LNR 28MM HWALL SZ23
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·August 21, 2020
28MM DIA COCR MOD HD +9MM NK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·August 21, 2020
NITE GUARD
FDA Adverse Event
Malfunction
·RANIR LLC·Product code OBR·May 1, 2014
PROLENE POLYPROPYLENE MESH
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·May 15, 2013
VASOVIEW HEMOPRO 2 EVH SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·May 17, 2011
BI-METRIC CDH POR N/C 7X114
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·February 28, 2019
M2A 38MMX56MM CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 28, 2019
M2A 38MM MOD HD -6MM NK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 28, 2019
R3 XLPE INSERT
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JDI·May 25, 2025
BI-METRIC CDH POR N/C 7X114
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·February 27, 2019
TITANIUM SCREW LOW PROF 5X25MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·February 27, 2019
TITANIUM SCREW LOW PROF 5X30MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·February 27, 2019