51 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Fixion Nailing System
FDA UDI
CARBOFIX ORTHOPEDICS LTD·07290109330716·An interlocking intramedullary nail intended fo...
Fixion Nailing System
FDA UDI
CARBOFIX ORTHOPEDICS LTD·07290109330006·The nail is intended for use in the fixation of...
MIRABAY
FDA UDI
Mirabay Orthodontics Corp.·05061075022996·KLEOS 2 PSL METAL MBT 022 LR5 PK5
CORTICAL BONE SCREW 3.5mm x 18mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665033168·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694039901·PrimaLIF Small Cobb, Straight
Avalign
FDA UDI
Avalign Technologies, Inc.·00190776020811·Keyhole Bracket
22mm x 10mm x 18mm PLIF with Inserter
FDA UDI
XENCO MEDICAL LLC·B064XM01100181·22mm x 10mm x 18mm PLIF
CARDICA C-PORT XA PLUS DISTAL ANASTOMOSIS SYSTEM, MODEL FG-000100
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
GOLIFE NASAL MASK
FDA 510(k)
FDA Class 2
·Anesthesiology
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·January 7, 2025
MR850
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 11, 2026
FISHER AND PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE·Product code BTT·September 22, 2025
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 6, 2024
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·December 10, 2024
FISHER AND PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE·Product code BTT·November 4, 2025
FISHER AND PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE·Product code BTT·November 19, 2025
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·June 10, 2024
RESPIRATORY HUMIDIFIER
FDA Adverse Event
Injury
·Product code BTT·February 18, 2021
RADICAL 7
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·December 18, 2014