510(k) K251988

Device
Boston iFace (Boston iFace)
Applicant
Boston Aesthetics, Inc.
510(k) number
K251988
Product code
GEI
Decision
Substantially Equivalent (SESE)
Decision date
2026-01-12
Date received
2025-06-27
Regulation
878.4400
Classification name
Electrosurgical, Cutting & Coagulation & Accessories
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Hongmei Cao
Address
1521 Concord Pike Suite 201 Wilmington De 19803 Wilmington DE US 19803 19803

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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