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

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ZYBIT

FDA 510(k)
FDA Class 2 ·Cardiovascular

ACE

FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950023684·RONGEUR HARTMAN CURVED 4MM WIDE 6-1/2" 16.5CM

artVeneer life

FDA UDI
Merz Dental GmbH·D7092002004·artVeneer life upper posteriors, M, A1

BEMIS

FDA UDI
BEMIS MANUFACTURING COMPANY·10073088150551·800CC HIFLOW SOLO SUCTION CANISTER WITH AEROSTA...

APOLLO Ankle Fracture Plating System

FDA UDI
Glw, Inc.·18435711003214·APOLLO Ankle Fracture Plates / Posterior Plate ...

APOLLO Ankle Fracture Plating System

FDA UDI
Glw, Inc.·18435711003221·APOLLO Ankle Fracture Plates / Posterior Plate ...

Battalion

FDA UDI
ALPHATEC SPINE, INC.·00840967188461·Battalion, LLIF Trial, 0°, 20 mm Wide, 04 mm X ...

DULBECCO'S MODIFIED EAGLE'S MEDIUM, NO. 200-2004

FDA 510(k)
FDA Class 1 ·Hematology

KineMatch® PFR System

FDA UDI
Kinamed, Inc.·00818720010908·DRILL GUIDE LEFT

MONTANE TATRAS M-S2.F0 [SZER 69 CM]

FDA UDI
MEDEN INMED SP Z O O·05903684801428·The MONTANE treatment table is a treatment tabl...

ALLIANCE LEFT HEART DELIVERY SYSTEM INTRODUCER, MODEL #407509

FDA 510(k)
FDA Class 2 ·Cardiovascular

WIN-1 TANGO

FDA 510(k)
FDA Class 2 ·Physical Medicine

*

FDA Adverse Event
Injury ·MCKINLEY MEDICAL·Product code MEB·July 9, 2008

SPECIALITE

FDA Adverse Event
Malfunction ·HILL-ROM ARCHITECTURAL PRODUCTS/HILL-ROM CO. INC.·Product code KZF·December 19, 2006

SPECIALITE

FDA Adverse Event
Other ·HILL-ROM CO. INC, HILL-ROM ARCHITECTURAL PRODUCTS·Product code KZF·February 12, 2007

SYRINGE 0.3ML 31GA 8MM TW 10BAG 500 CA

FDA Adverse Event
Malfunction ·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·May 14, 2024

SYRINGE 0.3ML 31GA 8MM TW 10BAG 500 CA

FDA Adverse Event
Malfunction ·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·May 14, 2024

XENFORM

FDA Adverse Event
Other ·TEI BIOSCIENCES INC.·Product code FTM·March 11, 2013

TOTALCARE BARIATRIC BED

FDA Adverse Event
Malfunction ·HILL-ROM INC.·Product code IOQ·July 3, 2014

MULTI-LINK RX PIXEL CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·February 22, 2008