66 results · 23ms · Sources: EU EUDAMED, US FDA

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Stryker ICONIX with Needles

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772813148·GENUMEDI PRO SILVER SIZE I

ResinBlend LV Composite Blending Resin

FDA UDI
DEN-MAT HOLDINGS, LLC·00359883003791·Dental unfilled resin sealant/coating

Oticon

FDA UDI
Oticon A/S·05707131280251·H11, DESIGNRITE 10 WL CRED

ResinBlend LV Composite Blending Resin

FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172017084·Dental unfilled resin sealant/coating

STRYKER

FDA UDI
MAKO SURGICAL CORP.·07613327409086·MAKO KNEE TRAY BASE

Brasseler USA

FDA UDI
Peter Brasseler Holdings, LLC·00887919890218·RESINBLEND LV 3ML/BOTTLE 1P

General Instruments

FDA UDI
ALPHATEC SPINE, INC.·00840180526132·A-ARM ADAPTOR, M-TUBE, LTP

LEONE SPA

FDA UDI
LEONE SPA·08033707071495·MINI ORTHODONTIC IMPLANT LOW D1,5 L12 mm

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575289769·Orthopaedic implant aiming/guiding block, reusa...

n/a

FDA UDI
Ortho Development Corporation·00822409070459·Snap-on Fem Augment Trial 12mm Distal Size 5

E1 MEDICAL FLAT PANEL DISPLAY SYSTEM AND MFGD 1218 MEDICAL FLAT PANEL DISPLAY

FDA 510(k)
FDA Class 2 ·Radiology

STRAIGHT ABUTMENT, 4.2, 4.6, 5.0, 6.4, IMPLANT 6.0, IMPLANT 7.0, IMPLANT 8.0 MODEL: 002061, 002062, 002063, 002064,

FDA 510(k)
FDA Class 2 ·Dental

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 12, 2024

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

COGNIS

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 6, 2011

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORPORATION·Product code DZC·September 9, 2008

SPECTRANETICS QUICK-CROSS SUPPORT CATHETER

FDA Adverse Event
Injury ·THE SPECTRANETICS CORPORATION·Product code DQY·March 6, 2019

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025