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Magma Spark

FDA UDI

Class II (US FDA UDI)

by Formatk Systems Ltd

Identity

Trade Name
Magma Spark FDA UDI
Generic Name
Dermatological diode laser system FDA UDI
Device Name
Magma Spark system supprting Laser applicators indicated for various treatments such as Hair Removal, Permanent Hair Reduction and pseudofolliculitis babae (PFB) FDA UDI
Model / Reference
FS80000 FDA UDI
Description
Magma Spark system supprting Laser applicators indicated for various treatments such as Hair Removal, Permanent Hair Reduction and pseudofolliculitis babae (PFB) FDA UDI

Identifiers

Catalog Number
FS80000 FDA UDI
Primary DI / UDI-DI
07290016681031 FDA UDI
510(k) Number
K162781 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Dermatological diode laser system 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dermatological diode laser system

Magma Spark by Formatk Systems Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatological diode laser system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Formatk Systems Ltd

Sources (1)

  • FDA UDI ecd1a43a-4530-42bc-b918-44ee7d160a22 35 fields · synced May 30, 2026