Soliton, Inc. FDA Approvals

0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
Resonic Rapid Acoustic Pulse Device510(k)Nov 5, 2021General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Nov 5, 2021
Resonic Rapid Acoustic Pulse Device510(k)Apr 27, 2021General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Special)	Apr 27, 2021
Rapid Acoustic Pulse Device510(k)Jan 29, 2021General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Jan 29, 2021