629 results
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17ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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KAHOOK DUAL BLADE GLIDE
FDA Adverse Event
Injury
·NEW WORLD MEDICAL, INC.·Product code QUQ·January 27, 2026
Knife, Intraocular Pressure Lowering
FDA classification
FDA Class 2
·Knife, Intraocular Pressure Lowering
Scaler Tip 3UQ
FDA UDI
W & H Dentalwerk Bürmoos GmbH·J021080239401·Tip 3UQ with changer
Scaler Tip 2UQ
FDA UDI
W & H Dentalwerk Bürmoos GmbH·J021080239301·Tip 2UQ with tip changer
Scaler Tip 1UQ
FDA UDI
W & H Dentalwerk Bürmoos GmbH·J021080239201·Tip 1UQ with tip changer
QNQ Design and Development Pvt. Ltd.
FDA registration
QNQ Design and Development Pvt. Ltd.·4 products·🇮🇳 India
AFFINITY QS Q-SWITCHED ND:YAG LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
4FUSION
FDA UDI
Stryker GmbH·07613252263173·4-Fusion Fixation Device
4FUSION
FDA UDI
Stryker GmbH·07613252263159·4-Fusion Fixation Device
4FUSION
FDA UDI
Stryker GmbH·07613252263180·4-Fusion Fixation Device
Luminance RED Tip
FDA UDI
Luminance Medical Ventures Incorporated·00860002593074·
Coal Black Polymer
FDA UDI
JBC and Company·D851QQ0·Tinted Opaque Powder
SPECTRA QT: Q-SWITCHED ND: YAG LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ANALYZER: NOVA STAT PROFILE 1 QUA CON MAT: ELECT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Human Touch
FDA UDI
Human Touch, LLC·00045915829636·A mains electricity (AC-powered) device specifi...
Human Touch
FDA UDI
Human Touch, LLC·00045915829643·A mains electricity (AC-powered) device specifi...
PERCEVAL SUTURELESS AORTIC HEART VALVE
FDA Adverse Event
Death
·CORCYM CANADA CORP.·Product code LWR·September 1, 2021
OPTI [QUE] BALLOON
FDA Adverse Event
Other
·ABBOTT LABORATORIES·Product code DQO·January 2, 2004
QN-Q SILVERSOAKER
FDA Adverse Event
Injury
·I-FLOW CORP.·Product code MEB·May 12, 2009
C-QUE MESH
FDA Adverse Event
Injury
·ATRIUM MEDICAL CORP.·Product code FTL·September 11, 2014