19 results · 20ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

GENESIS MEDICAL INTERVENTIONAL F.A.S.T. (FACILITATED ASPIRATION/SUCTION THROMBECTOMY) SYSTEMS

FDA 510(k)
FDA Class 2 ·Cardiovascular

20GA Illuminating Laser Probe, SMA905

FDA UDI
Peregrine Surgical, Llc·00632307001758·20GA Illuminating Laser Probe, SMA905

Ormco

FDA UDI
ORMCO CORPORATION·00889989024739·BONDABLE LINGUAL RETAINER CUSPID O

n/a

FDA UDI
Ortho Development Corporation·00822409073757·10/12 Distal Reamer 10mm

Trulink

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522126277·CO2 NASAL CANNULA, ADULT

LEONE SPA

FDA UDI
LEONE SPA·08033707001959·LEOWIRE SPRING HARD 1,0mm

eWave 6-Lead EKG

FDA UDI
Wearlinq, Inc.·K00010·Continuous wearable electrocardiogram (ECG) mon...

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR21020400101·Compound retraction arch max. .016"x.022" / 45°

Aspida

FDA UDI
ALPHATEC SPINE, INC.·00811801038334·Adjustable ASPIDA Driver

DRIVEMEDICAL

FDA UDI
Drive Devilbiss Healthcare·50822383525148·Canes & CrutchesCrutches Product Description: E...

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710820400100·Zadik Calcaneal Guide, 40mm x 10°

ACCU-CHEK COMPACT SYSTEM, ACCU-CHEK COMPACT TEST STRIPS, ACCU-CHEK COMPACT COMPACT CONTROLS

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

VALLEYLAB LIGASURE PRECISE INSTRUMENT VESSEL SEALING SYSTEM-MODEL # LS1200 & SLIGAURE GENERATOR

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

TESS GLENOID REVERSE HEAD DIAMETER 36

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·October 27, 2016

REMSTAR AUTO M SERIES

FDA Adverse Event
Injury ·RESPIRONICS, INC.·Product code BZD·April 14, 2024

3I T3® WITH DCD® TAPERED IMPLANT 5/4 X 10MM

FDA Adverse Event
Injury ·BIOMET 3I·Product code DZE·June 26, 2019

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·April 8, 2013

ACCU-CHEK SPIRIT COMBO

FDA Adverse Event
Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·March 9, 2011

LCS R BRDG BRG STD+/LG 12.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·May 6, 2008