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

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CA-1500

FDA 510(k)
FDA Class 2 ·Radiology

GEN4 DIGITAL

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828132848·GEN4 DIGITAL

CosmoLock

FDA UDI
Kalitec Direct LLC·B073DRK0100280·Tab Breaker, Single Sided, Cosmolock MIS

Intess C

FDA UDI
Kalitec Direct LLC·B07309K0100280·Caddie Lid, Cervical Implants, Hinged

Navagio

FDA UDI
Kalitec Direct LLC·B07330K0100280·Caddie, 32-36mm Curved Cages

Cosmolock

FDA UDI
Kalitec Direct LLC·B07310K0100280·Caddie, MIS Rods and Caps

Disposable Cuff

FDA UDI
SUNTECH MEDICAL, INC.·10840935106364·

DENTURE BASE

FDA UDI
AMERICAN TOOTH INDUSTRIES·D772ATI0400280·DENTURE BASE REGULAR FIBERED 7 LB

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710410400280·Anterior Closing Wedge Osteotomy Guide, 40mm x ...

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710400400280·Anterior Dome Osteotomy Guide, 40mm x 28mm

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710420400280·Anterio Lateral Closing Wedge Osteotomy Guide, ...

Sensor, Electro-Optical (For Cervical Cancer)

FDA Pre-Market Approval
FDA Class 3 ·LUMA CERVICAL IMAGING SYSTEM

CONTOUR CURVED CUTTER STAPLER CS

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 13, 2006

RENAFLO II HF 2000 HEMOFILTER

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

ARGLAES-AB ANTIMICROBIAL BARRIER POWDER DRESSING

FDA 510(k)
FDA Unclassified ·Unknown

GEMSTAR PAIN MGE SNG

FDA Adverse Event
Malfunction ·HOSPIRA, INC.·Product code MEA·November 12, 2009

Sensor, Electro-Optical (For Cervical Cancer)

FDA Pre-Market Approval
FDA Class 3 ·LUMA CERVICAL IMAGING SYSTEM

Sensor, Electro-Optical (For Cervical Cancer)

FDA Pre-Market Approval
FDA Class 3 ·CERVICAL IMAGING SYSTEM

Sensor, Electro-Optical (For Cervical Cancer)

FDA Pre-Market Approval
FDA Class 3 ·LUMA CERVICAL IMAGING SYSTEM

Sensor, Electro-Optical (For Cervical Cancer)

FDA Pre-Market Approval
FDA Class 3 ·LUMA CERVICAL IMAGING SYSTEM