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Dp Dermaceuticals L.E.D. FACE

FDA UDI

Class II (US FDA UDI)

by iSMART Developments, Ltd.

Identity

Trade Name
Dp Dermaceuticals L.E.D. FACE FDA UDI
Generic Name
Cosmetic red-light phototherapy system, home-use FDA UDI
Device Name
v2 Facemask- DP Dermaceuticals Branded FDA UDI
Model / Reference
TN19G FDA UDI
Description
v2 Facemask- DP Dermaceuticals Branded FDA UDI

Identifiers

Catalog Number
111B FDA UDI
Primary DI / UDI-DI
05060534510104 FDA UDI
510(k) Number
K191629 FDA UDI
FDA Product Code
OHS FDA UDI
GMDN Term
Cosmetic red-light phototherapy system, home-use 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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cosmetic red-light phototherapy system, home-use

Dp Dermaceuticals L.E.D. FACE by iSMART Developments, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cosmetic red-light phototherapy system, home-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f0cfab94-1d79-462a-b788-36daab3c185a 36 fields · synced May 30, 2026