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

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CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0310080·Probe, 1.5 inch Ball, Lenke, Thoracic, Straight...

AESCULAP NEURO PATTIES, NEUROSORB 4, 6, AND 75 (GREEN & WHITE)

FDA 510(k)
FDA Class 2 ·Neurology

AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 8mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665009248·

EVOS Lumbar Interbody System

FDA UDI
Cutting Edge Spine, LLC·00841193107707·HA PEEK EVOS Straight, ,8mmx11mmx 30mm , FLAT 5...

IVF HARTMANN AG

FDA registration
IVF HARTMANN AG·1 product·🇨🇭 Switzerland

K032008

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code LJT·May 31, 2007

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710620310080·Quad Channel Met-Traverse, 31mm x 8mm

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710610310080·Tri-Channel Met-Traverse, 31mm x 8mm

NEXUS 2 MODIFIED

FDA 510(k)
FDA Class 2 ·Dental

TEMPTELLER INFRARED EAR THERMOMETER, MODELS TT-901, TT-911 AND TT-921

FDA 510(k)
FDA Class 2 ·General Hospital

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·April 2, 2019

SEE H10

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

BRAVO

FDA Adverse Event
Malfunction ·GIVEN IMAGING LTD.·Product code FFT·March 28, 2013

ACCU-CHEK SPIRIT

FDA Adverse Event
Injury ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·March 16, 2011

GE OEC 9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 17, 2008

ALINITY M RESP-4-PLEX AMP KIT

FDA Adverse Event
Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025

ALINITY M RESP-4-PLEX AMP KIT

FDA Adverse Event
Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025

ALINITY M RESP-4-PLEX AMP KIT

FDA Adverse Event
Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025

ALINITY M RESP-4-PLEX AMP KIT

FDA Adverse Event
Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025

ALINITY M RESP-4-PLEX AMP KIT

FDA Adverse Event
Malfunction ·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025