26 results · 22ms · Sources: EU EUDAMED, US FDA

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OrthoScan TAU Mini C-Arm

FDA 510(k)
FDA Class 2 ·Radiology

Vanguard® Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304439566·

BOSS Instruments

FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515028210·Balfour Abdominal Ret set, 7 1/8" spread, fixed...

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668100974·DESMARRES LID RETRACTOR #2

EMERGE PTCA DILATATION CATHETER (MONORAIL) EMERGE PTCA DILATATION CATHETER (OVER-THE-WIRE)

FDA 510(k)
FDA Class 2 ·Cardiovascular

VOYAGER PERITONEAL DIALYSIS SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

EMERGE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·November 27, 2024

EMERGE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 29, 2025

EMERGE?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·May 19, 2026

EMERGE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 8, 2026

EMERGE?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 30, 2026

EMERGE?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·January 30, 2026

EMERGE?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·October 28, 2025

EMERGE?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·February 26, 2026

EMERGE?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·April 21, 2026

COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 3, 2008

MONOPOLAR CURVED SCISSORS INSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 21, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

ENDOPATH XCEL TROCAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·November 19, 2019

ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 27, 2019