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dpl®

FDA UDI

Class II (US FDA UDI)

by Led Technologies, Inc.

Identity

Trade Name
dpl® FDA UDI
Generic Name
Blue/red/infrared phototherapy lamp FDA UDI
Model / Reference
FLEXPAD FDA UDI

Identifiers

Primary DI / UDI-DI
B347FLEXPAD0 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Blue/red/infrared phototherapy lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 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

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: Blue/red/infrared phototherapy lamp

dpl® by Led Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blue/red/infrared phototherapy lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 60462bbf-4de6-4916-9064-cf6c2d23f3d7 32 fields · synced May 30, 2026