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Unipolar HP

FDA UDI

Class II (US FDA UDI)

by Alma Lasers Ltd.

Identity

Trade Name
Unipolar HP FDA UDI
Generic Name
Radio-frequency skin/body contouring system FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Catalog Number
AASR11021407 FDA UDI
Primary DI / UDI-DI
17290110121614 FDA UDI
510(k) Number
K160075 FDA UDI
FDA Product Code
NUV FDA UDI
ISA FDA UDI
GMDN Term
Radio-frequency skin/body contouring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
890.5660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radio-frequency skin/body contouring system

Unipolar HP by Alma Lasers Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radio-frequency skin/body contouring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alma Lasers Ltd.

Sources (1)

  • FDA UDI 59b07e47-1ecb-4547-859d-6c1d302b022c 34 fields · synced May 31, 2026