10,000 results
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94ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EMERSON MODEL 3MV-OAA ALARM MODULE
FDA 510(k)
FDA Class 2
·Anesthesiology
SCORPIO NRG CR FEMORAL COMPONENT WITH HA SIZE 5
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·September 12, 2007
MEDLINE
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES, INC.·Product code FMI·October 11, 2019
MPS 3 ND Delivery Set w/o AA w/305cm Line (16C)
FDA UDI
QUEST MEDICAL INC·00634624530362·
UNK CENTRAL SCREW
FDA Adverse Event
Injury
·TORNIER INC·Product code KWS·May 26, 2026
UNK GLENOID BASEPLATE
FDA Adverse Event
Injury
·TORNIER INC·Product code KWS·May 22, 2026
LOGIC TIBIA PS MOD INSRT SZ 3.5 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 5, 2020
ONYX
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·June 13, 2019
UNKNOWN_TIBIAL BASEPLATE
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·March 13, 2023
CAREFUSION
FDA Adverse Event
Other
·CAREFUSION·Product code BZD·September 17, 2012
DIAMONDBACK PERIPHERAL ORBITAL ATHERECTOMY SYSTEM
FDA Adverse Event
Injury
·CARDIOVASCULAR SYSTEMS, INC.·Product code MCW·March 28, 2022
ONYX
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 22, 2019
EUFLEXXA
FDA Adverse Event
Injury
·BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.·Product code MOZ·April 8, 2022
PLASTIC BILIARY STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 26, 2024
SUPARTZ
FDA Adverse Event
Injury
·SEIKAGAKU CORP.·Product code MOZ·March 15, 2013
EUFLEXXA
FDA Adverse Event
Injury
·BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.·Product code MOZ·March 3, 2023
ONYX AVM
FDA Adverse Event
Malfunction
·COVIDIEN (IRVINE)·Product code MFE·March 23, 2018
EUFLEXXA
FDA Adverse Event
Injury
·BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.·Product code MOZ·April 8, 2015
Aid, Visual, For Nausea
FDA classification
FDA Not Classified
·Aid, Visual, For Nausea
AOA PRODUCTS LLC
FDA registration
AOA PRODUCTS LLC·1 product·🇺🇸 United States