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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

SOLOCEM

FDA 510(k)
FDA Class 2 ·Dental

SoloPace Fusion Sterile Pack

FDA UDI
SOLO PACE INC.·00850056280044·

LITE ART

FDA 510(k)
FDA Class 2 ·Dental

FIXED BEARING UNI COMPONENT

FDA 510(k)
FDA Class 2 ·Orthopedic

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 12, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 11, 2024

BIPAP A40

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 9, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 6, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 13, 2024

IDENTITY ADX DR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 13, 2014

UNIDENTIFIED ZIRCONIA HEAD 28MM + 8.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS·Product code KWA·May 21, 2013

ASR UNI FEMORAL IMPL SIZE 55

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 2, 2011

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 16, 2024

BIPAP A40 PRO, IT

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 5, 2025

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·June 5, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·June 6, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·June 5, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 11, 2024

BIPAP A40 PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 11, 2024

BIPAP A40

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code MNT·September 11, 2024