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Gsd

FDA UDI

Class II (US FDA UDI)

by Shenzhen GSD Tech Co., Ltd.

Identity

Trade Name
GSD FDA UDI
Generic Name
Dermatological diode laser system FDA UDI
Model / Reference
GP900A FDA UDI

Identifiers

Primary DI / UDI-DI
06928258000907 FDA UDI
510(k) Number
K142186 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

Gsd by Shenzhen GSD Tech Co., 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

K142186 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1e89f796-f469-410e-8322-2795e619ec03 33 fields · synced May 30, 2026