38 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SiteSeal Femoral Compression Device
FDA 510(k)
FDA Class 2
·Cardiovascular
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304462991·
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260742·
Orthos
FDA UDI
ORMCO CORPORATION·00889989030358·ORTHOS CM TMA 021 X 025 UPLG PK10
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690198680·AK3 Ultra Insert Trial Size 4, 13mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694019118·2.4mm x 13mm Cannulated Lag Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070645·Cannulated 2.4 x 13mm Lag Screw Sterile Qty 5
FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL
FDA 510(k)
FDA Class 2
·Orthopedic
INVIROSNAP 50 AND 100 UNIT INSULIN SAFETY SYRINGES
FDA 510(k)
FDA Class 2
·General Hospital
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 17, 2025
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 22, 2025
JOSTENT GRAFTMASTER
FDA Adverse Event
Injury
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·October 7, 2008
LTV
FDA Adverse Event
Malfunction
·CAREFUSION 203, INC.·Product code CBK·June 18, 2013
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·August 5, 2011
MAXZERO NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FPA·January 6, 2020
M2A-MAGNUM PF CUP 52ODX46ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·March 23, 2022
M2A-MAGNUM 42-50MM TPR INSRT-6
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·March 23, 2022
M2A-MAGNUM MOD HD SZ 46MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·March 23, 2022
M2A-MAGNUM MOD HD SZ 46MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·September 8, 2021
M2A-MAGNUM PF CUP 52ODX46ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·September 8, 2021