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Mini Speed HP

FDA UDI

Class II (US FDA UDI)

by Alma Lasers Ltd.

Identity

Trade Name
Mini Speed HP FDA UDI
Generic Name
Ultrasonic skin/body contouring system FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Catalog Number
AAUL25101702 FDA UDI
Primary DI / UDI-DI
17290110121690 FDA UDI
510(k) Number
K160075 FDA UDI
FDA Product Code
NUV FDA UDI
ISA FDA UDI
IMI FDA UDI
GMDN Term
Ultrasonic skin/body contouring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
890.5660 FDA UDI
890.5300 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: Ultrasonic skin/body contouring system

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

Similar devices

Also classified as Ultrasonic 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 d5273776-9800-426a-b92e-bd10ac131e55 34 fields · synced May 31, 2026