12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARIETTA 50
FDA 510(k)
FDA Class 2
·Radiology
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017880·K-Wire, Double Ended, Trocar Point, Diameter Si...
Pre-Finisher
FDA UDI
TP ORTHODONTICS INC·00192029041864·2 Upper Bicuspid Extraction
CETRA
FDA UDI
Orthofix US LLC·18257200120468·2-LEVEL PLATE ASSEMBLY, 48MM
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306804342·Joseph Periosteal Elevator, 16.5cm
BIPAP AUTOSV
FDA 510(k)
FDA Class 2
·Anesthesiology
DRFP PROSMART ROOT CANAL OBTURATION SYSTEM, PROPOINTS 4% 6%, PT, S
FDA 510(k)
FDA Class 2
·Dental
BIPAP AUTOSV ADV
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNS·March 10, 2022
LGN XLPE PS INSERT SZ 5-6 9MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·October 21, 2014
6000CMS
FDA Adverse Event
Malfunction
·MOOG DEVICE GROUP·Product code FRN·June 10, 2013
IPUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011
ARROW CVC SET: 3-LUMEN 7FR X 20CM
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code FOZ·May 23, 2018