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Cellulize

FDA UDI

Class II (US FDA UDI)

by Photonica USA LLC

Identity

Trade Name
Cellulize FDA UDI
Generic Name
Low-intensity laser fat liquefaction system FDA UDI
Device Name
Cellulize, Green Light (532nm) FDA UDI
Model / Reference
60002 FDA UDI
Description
Cellulize, Green Light (532nm) FDA UDI

Identifiers

Catalog Number
60002 FDA UDI
Primary DI / UDI-DI
00860925000314 FDA UDI
510(k) Number
K180338 FDA UDI
FDA Product Code
OLI FDA UDI
GMDN Term
Low-intensity laser fat liquefaction system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5400 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Low-intensity laser fat liquefaction system

Cellulize by Photonica USA LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Low-intensity laser fat liquefaction system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Photonica USA LLC

Sources (1)

  • FDA UDI 96586311-5d21-4837-be72-67d3799d43aa 35 fields · synced May 30, 2026