24 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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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