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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