37 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
WellDoc BlueStar
FDA 510(k)
FDA Class 2
·General Hospital
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690195177·AK3 Femoral Distal Locating Device, Fixed Bushing
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101063·KNAPP RETRACTOR 4-PRONG SHARP
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·AED Battery Exchange (Models 9146-ABE, G5-ABE, 5070-ABE, FR3-ABE)
devemed
FDA UDI
devemed GmbH·04061644021284·Filling instrument, spatulate # 4
2.5 / 2.5 mm
...
Tap 5.5
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215039455·
Reicodent
FDA UDI
devemed GmbH·04061644050741·Filling instrument, spatulate # 4
2.5 / 2.5 mm
...
NA
FDA UDI
STRYKER CORPORATION·04546540373106·5.0mm XX-Coarse Diamond Round
NA
FDA UDI
STRYKER CORPORATION·04546540373090·4.0mm XX-Coarse Diamond Round
NA
FDA UDI
STRYKER CORPORATION·04546540373113·6.0mm XX-Coarse Diamond Round
NA
FDA UDI
STRYKER CORPORATION·04546540373120·7.0mm XX-Coarse Diamond Round
CHEMPAQ XBC ANALYZER
FDA 510(k)
FDA Class 2
·Hematology
TEMPSPAN CLEAR MATRIX
FDA 510(k)
FDA Class 2
·Dental
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·DBP-1400-ABE and DBP-2003- ABE
Reicodent
FDA UDI
devemed GmbH·04061644034925·Filling instrument, spatulate # 4
2.5 / 2.5 mm
...
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·March 13, 2026
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025