31 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HeartCheck Cardi Beat ECG Monitor with GEMS Mobile
FDA 510(k)
FDA Class 2
·Cardiovascular
Ultra Container
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482137703·Three Quarter Length, Steam Container, 18 X 13 ...
BI-METRIC X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304182745·
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704512694·
Ultra Container
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482137710·Three Quarter Length, Gravity Container, 18 X 1...
Symetri Clear
FDA UDI
ORMCO CORPORATION·00889989084566·U3R SYMETRI CLEAR MCLAUGHLIN, BENNETT & TREVISI...
BRUX MOUTHGUARDS
FDA 510(k)
FDA Unclassified
·Unknown
VU APOD INTERVERTEBRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
eTRAX™ Needle
FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436103517·Sterile needle, 18GA x 13cm with (7.6 tapered t...
GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·July 16, 2020
GMK-PRIMARY FEMUR PS CEMENTED SIZE 4
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 22, 2019
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981301064·Lollipop Trial, Right/Down-Angled, 18mm x 13mm ...
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981301019·Lollipop Trial, Right/Up-Angled, 18mm x 13mm x ...
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981300968·Lollipop Trial, Anterior-Angled, 18mm x 13mm x ...
GMK-PRIMARY FEMUR PS CEMENTED SIZE 4 LEFT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·August 23, 2017
GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·September 25, 2018
KINETRA
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·July 21, 2011
HUDSON CONCHA NEPTUNE
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTT·June 7, 2013
SOFTCLIX PLUS LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·September 23, 2008
BLUNT TIP SCREW, ÿ 4X48MM
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code HSB·May 20, 2024