Liposense 150mm cannula only with case

FDA UDI

Class II (US FDA UDI)

by Alma Lasers Ltd.

Identity

Trade Name: Liposense 150mm cannula only with case FDA UDI
Generic Name: Liposuction system cannula, reusable FDA UDI
Model / Reference: 1 FDA UDI

Identifiers

Catalog Number: AALS11012302 FDA UDI
Primary DI / UDI-DI: 07290110123079 FDA UDI
510(k) Number: K212073 FDA UDI
FDA Product Code: GEX FDA UDI
GMDN Term: Liposuction system cannula, reusable FDA UDI

Classification

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

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Liposuction system cannula, reusable

Liposense 150mm cannula only with case by Alma Lasers Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K212073 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Alma Lasers Ltd.

Sources (1)

FDA UDI 363c11d8-723a-4ab2-bb5b-f845005725af 34 fields · synced May 30, 2026