FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Ulthera® System

K Number: K260618 · Decision May 21, 2026
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
29
Applicant Total
14
Review Days
85

Basic Information

Device Name
Ulthera® System
K Number
K260618
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4590
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ulthera, Inc.
Date Received
February 25, 2026
Decision Date
May 21, 2026
Product Code
OHV
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OHV Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OHV), ordered by most recent decision date.

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Other Clearances by Ulthera, Inc.

K Number Device Name
K250418 Ulthera System (UC-1 Control Unit PRIME Model 2.1)
K243035 Ulthera® System
K233996 Ulthera System (UC-1 Control Unit PRIME)
K192185 The Cellfina System
K180623 Ulthera System
K161885 The Cellfina System
K153677 The Cellfina System
K150505 Cellfina System
K134032 ULTHERA SYSTEM
K132028 ULTHERA SYSTEM
Search all 14 clearances from Ulthera, Inc. →