22 results · 21ms · Sources: EU EUDAMED, US FDA

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EYE APPLICATORS CAT.#980-983

FDA 510(k)
FDA Class 1 ·General Hospital

Total Foot System 2

FDA UDI
Smith & Nephew, Inc.·00885556838051·REAR FOOT UNIVERSAL PLATE. 16MM

Integra® Total Foot System

FDA UDI
Ascension Orthopedics, Inc.·10381780119319·The Integra Total Foot System Universal Rearfoo...

Two Striper

FDA UDI
ABRASIVE TECHNOLOGY, INC.·B868C8020161·Dental Root Canal Post

Bardia® Closed System Foley Catheter Tray

FDA UDI
C. R. Bard, Inc.·00801741019678·Bardia® Closed System Foley Catheter Tray with ...

Vista Short High Volume Aspirator 11.5 x 7.5 mm

FDA UDI
Vista Dental·10818207021585·

Symmetry Surgical

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482032275·Symmetry® Scissors, Micro, Curved, Sharp/Sharp,...

ACUMED

FDA UDI
Acumed LLC·10806378052989·1.5 mm Depth Gauge 6-46 mm

n/a

FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM51008023140161·Rotary diamond instrument for dental application

XENFORM SOFT TISSUE REPAIR MATRIX

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code PAJ·May 4, 2015

PHILIPS INTEGRIS ALLURA

FDA 510(k)
FDA Class 2 ·Radiology

GDX VCC WITH ECC SOFTWARE

FDA 510(k)
FDA Class 2 ·Ophthalmic

TENSION FREE VAGINAL TAPE - ABBREVO UNKNOWN PROD

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·October 30, 2019

DUODERM/GRANUFLEX/DUOACTIVE-MOISTURE RETENTIVE

FDA Adverse Event
Malfunction ·CONVATEC INC.·Product code NAD·February 12, 2014

36MM MODULAR HEAD TYPE I TAPER MINUS 6MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·October 23, 2012

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code MDS·August 16, 2010

SPECTRA OPTIA

FDA Adverse Event
Injury ·TERUMO BCT·Product code LKN·March 13, 2020

SPECTRA OPTIA

FDA Adverse Event
Injury ·TERUMO BCT·Product code LKN·March 13, 2020

BD PLASTIPAK¿ LUER-SLIP SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 24, 2018

DORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)

FDA Enforcement
Class II ·Ongoing·Pro-Med Instruments Gmbh·June 4, 2025