42 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SUNI MAX
FDA 510(k)
FDA Class 1
·Dental
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950018093·FORCEP TISSUE DEBAKEY 2MM WIDE 7-3/4" 19.5CM
Bio2 Technologies
FDA UDI
BIO2 TECHNOLOGIES, INC.·B01010000491·VITRIUM E
22 x 7
Golvo™ mobile lift
FDA UDI
Liko AB·00887761981751·Mobile patient lifting system, battery-powered
Smile stretcher-purple bag
FDA UDI
Access Dental Lab, LLC·00850007728342·Smile stretcher in foil purple pouch
XS-100 Generator
FDA UDI
Philips Medical Systems DMC GmbH·00884838103795·X-ray control and HV generator
49mm Single-Use Acetabular Reamer
FDA UDI
Osteofit LLC·00850032869133·
QB1 NMES System
FDA UDI
Motive Health, Inc.·00854816006233·QB1 Post-Op Brace, NMES System; MEDIUM, SHORT, ...
SINGLE SIZE TENDON SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
SPIRAL RADIUS RODDING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·CARDIOSEAL SEPTAL OCCLUSION SYSTEM WITH QWIKLOAD
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 7, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·June 7, 2021
GOLVO MOBILE LIFT
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FSA·March 6, 2026
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·CARDIOSEAL
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·CARDIOSEAL SEPTAL OCCLUSION SYSTEM WITH QWIKLOAD
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·CARDIOSEAL SEPTAL OCCLUSION SYSTEM WITH QUICK LOAD
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·CARDIOSEAL SEPTAL OCCULUSION SYSTEM WITH QWIK LOAD
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·CARDIOSEAL SEPTAL OCCLUSION SYSTEM
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·CARDIOSEAL SEPTAL OCCLUSION SYSTEM WITH QWIKLOAD