1,900 results · 25ms · Sources: EU EUDAMED, US FDA

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INBODY BWA, INC.

FDA registration
INBODY BWA, INC.·8 products·🇺🇸 United States

ATUNE CR RT MS INS SZ 7 6

FDA Adverse Event
Injury ·DEPUY IRELAND - 3015516266·Product code JWH·December 26, 2025

PROX*ACCESS 55MM

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 5, 2009

BARDEX LUBRICATH PEDIATRIC FOLEY CATHETER

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·September 30, 2021

AMBIENT SUPER MULTIVAC 50 IFS

FDA Adverse Event
Malfunction ·ARTHROCARE CORP.·Product code BWA·September 2, 2015

DYONICS RF-S WHIRLWIND 90 DEG

FDA Adverse Event
Injury ·ARTHROCARE CORP.·Product code BWA·August 24, 2015

SUPER TURBOVAC 90

FDA Adverse Event
Malfunction ·ARTHROCARE CORP.·Product code BWA·August 24, 2015

COBLATOR II CONTROLLER

FDA Adverse Event
Injury ·ARTHROCARE CORP.·Product code BWA·September 2, 2015

VALLEYLAB

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code BWA·October 12, 2017

COBLATOR II

FDA Adverse Event
Malfunction ·ARTHROCARE CORP.·Product code BWA·September 8, 2015

AMBIENT SUPER TURBOVAC 90 IFS

FDA Adverse Event
Malfunction ·ARTHROCARE CORP.·Product code BWA·September 2, 2015

SURGITRON

FDA Adverse Event
ELLMAN INT'L INC.·Product code BWA·June 13, 2007

VALLEYLAB

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code BWA·September 6, 2024

VALLEYLAB

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code BWA·September 9, 2024

ELECTROSURGICAL GENERATOR

FDA Adverse Event
Injury ·VALLEY LAB,INC.·Product code BWA·June 22, 1992

ELECTROSURGICAL UNIT

FDA Adverse Event
Malfunction ·VALLEYLAB, INC.·Product code BWA·May 29, 1992

ELECTROSURGICAL PENCIL

FDA Adverse Event
Injury ·STERILE CONCEPTS/BIRTCHER·Product code BWA·February 23, 1995

VALLEYLAB

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code BWA·September 27, 2023

VALLEYLAB

FDA Adverse Event
Malfunction ·COVIDIEN MFG DC BOULDER·Product code BWA·May 20, 2024

VALLEYLAB

FDA Adverse Event
Malfunction ·COVIDIEN·Product code BWA·November 10, 2025