27 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Custodiol HTK Solution
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517576439·CoRoent Ant TLIF Ti, 9x12x40mm 8°
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260698·
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304463271·
Orthos
FDA UDI
ORMCO CORPORATION·00889989030327·ORTHOS CM TMA 016 X 022 UPLG PK10
OsteoMed
FDA UDI
OSTEOMED LLC·00845694009669·2.4mm x 8mm Cannulated Lag Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070546·Cannulated 2.4 x 8mm Lag Screw Sterile Qty 5
RHYTHM OF LIFE, MODEL R0901-05
FDA 510(k)
FDA Class 2
·Cardiovascular
DIGITAL DIAGNOSTIC X-RAY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
MIDWEST LOW SPEED ATTACHMENTS - CONTRA ANGLE SHEATH
FDA Adverse Event
Malfunction
·SIRONA DENTAL SYSTEMS GMBH·Product code EFB·April 20, 2023
OPTIPAC 60 REFOB BONE CMT R-3
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LOD·May 11, 2026
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 27, 2013
BHR
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·August 5, 2011
ESSURE
FDA Adverse Event
Other
·CONCEPTUS, INC.·Product code HHS·September 30, 2008
BIOMET BONE CMENT R 1X40 JP
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code LOD·May 22, 2025
REFOBACIN BONE CEMENT R 1X40-3
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code LOD·June 18, 2025
OPTIPAC 80 BIOMET BC R
FDA Adverse Event
Death
·BIOMET FRANCE S.A.R.L.·Product code LOD·April 9, 2026
BIOMET BONE CEMENT R 40 -3
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code LOD·July 31, 2025
BIOMET BONE CMENT R 1X40 JP
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code LOD·June 17, 2025
OPTIPAC 60 REFOB BONE CMT R-3
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LOD·February 5, 2025