24 results · 27ms · 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.

Modpod

FDA 510(k)
FDA Class 2 ·Physical Medicine

Genesis

FDA UDI
KEYSTONE DENTAL, INC.·D768K156950·Ratchet

Oticon

FDA UDI
Oticon A/S·05707131280473·NERA2 PRO, BTE 13 WL 85 DBL

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100622·KATENA DOUBLE-X SPECULUM V-WIRE

HNM Women Care

FDA UDI
HNM STAINLESS, LLC.·00812171028727·PESSARY, HODGE #2, W/SUPPORT, 75mm

COLLADENTAL BARRIER

FDA 510(k)
FDA Class 2 ·Dental

FLEX CONTROLLED PHOTOTHERAPY EQUIPMENT

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ATTUNE PS FEM LT SZ 8 CEM

FDA Adverse Event
Malfunction ·DEPUY IRELAND - 9616671·Product code OIY·March 23, 2021

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 19, 2025

PRECISION? MONTAGE? MRI

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 23, 2025

AXIOS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 17, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 20, 2025

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

ACCOLADE TMZF HIP STEM #4

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·June 6, 2013

TI CLICK'X LOCKING CAP FOR TI 3-D HEAD

FDA Adverse Event
Injury ·SYNTHES MONUMENT·Product code NKB·June 24, 2011

ATTUNE FEM POR PS RT SZ 8

FDA Adverse Event
Malfunction ·DEPUY IRELAND - 9616671·Product code NJL·May 10, 2021

AXIOS?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024

AXIOS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 27, 2024