16 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Avenir Muller Stem, Avenir Cemented Hip Stem
FDA 510(k)
FDA Class 2
·Orthopedic
Phasix
FDA UDI
Davol Inc.·00801741107641·Phasix Mesh, 12" x 12" (30 cm x 30 cm), Square
OsteoMed
FDA UDI
OSTEOMED LLC·00845694009881·3.0mm x 30mm Cannulated Lag Screw
Sklar®
FDA UDI
SKLAR CORPORATION·10649111023859·PLAIN SPLINTER FCP W/MAG 3"
SAIPH
FDA UDI
MATORTHO LTD·05055455506121·SAIPH Femur Cemented Blue Right Size 6
PIN SCREW
FDA UDI
BK MEDITECH CO.,LTD.·08809155854733·Wire Pin Screw, 3mm Shaft Diameter x 3mm Thread...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694071246·Cannulated 3.0 x 30mm Lag Screw Sterile Qty 5
COMPRESSOR NEBULIZER MODEL MCN-S600XX
FDA 510(k)
FDA Class 2
·Anesthesiology
SPINEOLOGY PEEK BULLET LUMBAR INTERBODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
SAIPH KNEE
FDA Adverse Event
Malfunction
·MATORTHO LIMTED·Product code JWH·October 3, 2019
G7 OSSEOTI MULTIHOLE 52MM E
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·December 16, 2021
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 27, 2013
QUANTUM TTC ESOPHAGEAL BALLOON DILATOR
FDA Adverse Event
Malfunction
·WILSON-COOK MED INC·Product code KNQ·July 22, 2011
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 22, 2014
HANDLE ACETABULAR PRESS
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025
ACETABULAR PRESSURIZER SMALL
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025