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

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EMS HEPA FILTER AND HME COMBINATIONS

FDA 510(k)
FDA Class 2 ·Anesthesiology

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033456064·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033456033·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033456019·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033456262·

InTess C Cervical Cage System

FDA UDI
Kalitec Direct LLC·B07309K01308N0·Cervical Rasp, 14 x 11, 8mm, 0 Degree, No Taper

Cosmolock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0130190·T-Handle, Head Persuader, 5.5mm

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033456040·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033456026·

BETHENNY EYEWEAR

FDA UDI
FGX INTERNATIONAL INC.·00193033456057·

EXCELSIOR MICROCATHETER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - CORK·Product code DQY·April 13, 2010

REAL PATIENT WIRELESS AMBULATORY EEG, MODEL EX-AMB-WIRELESS-RP (PROPOSED)

FDA 510(k)
FDA Class 2 ·Neurology

CHAD THERAPEUTICS OXYMATIC MODEL 401 AND OXYMATIC MODEL 411

FDA 510(k)
FDA Class 2 ·Anesthesiology

0009613348-2024-013089

FDA Adverse Event
Injury ·INSTITUT STRAUMANN AG·Product code DZE·October 3, 2024

CONTACT DETACH

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 19, 2025

CONTACT DETACH

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 19, 2025

CONTACT DETACH

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 19, 2025

TRUSTEEL

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 24, 2025

TRUSTEEL

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 24, 2025

EXCELSIOR MICROCATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - CORK·Product code DQY·May 18, 2010