510(k) K250524

Device
Mendaera Guidance System
Applicant
Mendaera, Inc.
510(k) number
K250524
Product code
ITX
Decision
Substantially Equivalent (SESE)
Decision date
2025-07-02
Date received
2025-02-21
Regulation
892.1570
Classification name
Transducer, Ultrasonic, Diagnostic
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Josh DeFonzo
Address
700 S Claremont St. Suite 200 San Mateo CA US 94402 94402

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00850062065086Mendaera Probe and Robot Drape KitMendaera, Inc.2025-08-11
10850062065069Mendaera Robot Drape KitMendaera, Inc.2025-08-11
10850062065045Mendaera Universal Instrument Guide Kit, ShortMendaera, Inc.2025-08-11
00850062065031Focalist System SoftwareMendaera, Inc.2025-08-11
10850062065021Mendaera Universal Instrument Guide Kit, LongMendaera, Inc.2025-08-11
00850062065000Focalist SystemMendaera, Inc.2025-08-11

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