45 results · 22ms · 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.

C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570

FDA 510(k)
FDA Class 2 ·Physical Medicine

PowerPICC SOLO

FDA UDI
Bard Access Systems, Inc.·00801741087431·Catheter Placement Kit

ASIA MED

FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282500221·asia-med Special No. 19: coated acupuncture ne...

ASIA MED

FDA UDI
asia-med GmbH·04251282507541·asia-med Special No. 19: coated acupuncture ne...

Bard Button Device Decompression Tube

FDA UDI
Bard Access Systems, Inc.·00801741080982·24 Fr. x 2.4 Button Decompression Tube

Zavation

FDA UDI
Zavation LLC·00842166122079·3-Level, 54mm Cervical Plate

RETAINER KIT

FDA UDI
Access Dental Lab, LLC·00850007728038·RETAINER KIT

Mariner MIS

FDA UDI
Seaspine Orthopedics Corporation·10889981182281·EXTENDED TAB BODY CT

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167700003540·

CURE™ ACP

FDA UDI
MEDITECH SPINE, LLC·B167S1700003540·

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·June 24, 2024

FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGEN

FDA 510(k)
FDA Unclassified ·Unknown

ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

TUFF IMPLANT

FDA Adverse Event
Injury ·NORIS MEDICAL LTD·Product code DZE·February 27, 2025

SURGISTOOL

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FZM·March 12, 2013

ACRYSOF

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·February 18, 2011

BIOPINCE

FDA Adverse Event
Malfunction ·MEDICAL DEVICE TECHNOLOGIES INC.·Product code KNW·January 18, 2008

HUDSON NEBULIZER ADAPTOR 033, STERILE, JAPANESE

FDA Adverse Event
Malfunction ·TELEFLEX·Product code CCQ·September 15, 2014

HUDSON NEBULIZER ADAPTER 033, STERILE, JAPANESE

FDA Adverse Event
Malfunction ·TELEFLEX·Product code CCQ·October 23, 2014

HUDSON NEBULIZER ADAPTOR 033, STERILE, JAPANESE

FDA Adverse Event
Malfunction ·TELEFLEX·Product code CCQ·October 23, 2014