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

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NEUWAVE Microwave Ablation System and Accessories

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

NA

FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252133735·ACTIVATION ROD FLEXIBLE, SHORT

OsteoMed

FDA UDI
OSTEOMED LLC·00845694006033·1.2mm Screwdriver Shaft, Long, Manual

DEBAKEY NEEDLE PULLING FORCEPS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896059566·DEBAKEY NEEDLE PULLING TISSUE FORCEPS TUNGSTEN ...

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112663·BARRON CORNEAL PUNCH 8.75MM

ENTEROSCOPY OVERTUBE, MODEL 00712140

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

MANUAL AND REMOTE CONTROLLED APPLICATOR SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

Widex

FDA UDI
Widex A/S·05706069689495·Widex BEYOND B-F2 (Tan silk ) Telecoil, RC coil...

Widex

FDA UDI
Widex A/S·05706069827255·WIDEX EVOKE EBB3D (Tan silk ) Telecoil, RC coil...

Widex

FDA UDI
Widex A/S·05706069424522·Widex MENU ME-9 BTE (Tan silk ) Telecoil, Volum...

Widex

FDA UDI
Widex A/S·05706069370393·Widex mind220 M2-9 BTE (Tan silk ) Telecoil, Vo...

PROTECTION SLEEVE FOR FNS INSERTION INSTRUMENTS

FDA Adverse Event
Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code GEA·January 27, 2021

SMR SHOULDER

FDA Adverse Event
Injury ·LIMACORPORATE S.P.A.·Product code MBF·July 25, 2025

NIBP CUFFS

FDA Adverse Event
Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code OED·March 5, 2026

VISIAN ICL (IMPLANTABLE COLLAMER LENS)

FDA Adverse Event
Malfunction ·STAAR SURGICAL COMPANY·Product code MTA·October 15, 2008

COLLEAGUE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011

CONSERVE(R) PLUS CUP

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·July 1, 2013

NIBP CUFFS

FDA Adverse Event
Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code OED·January 7, 2026

REVERSE #SHORT HUM. BODY 140°

FDA Adverse Event
Injury ·LIMACORPORATE S.P.A·Product code MBF·November 11, 2022

POWER STICK M5/3

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code GEY·March 10, 2025