← Back to catalogue

Boost LED Collar

FDA UDI

Class II (US FDA UDI)

by iSMART Developments, Ltd.

Identity

Trade Name
Boost LED Collar FDA UDI
Generic Name
Red/infrared light phototherapy unit FDA UDI
Device Name
Boost LED Collar- The Light Salon FDA UDI
Model / Reference
TN2113 FDA UDI
Description
Boost LED Collar- The Light Salon FDA UDI

Identifiers

Catalog Number
150-LS FDA UDI
Primary DI / UDI-DI
05060534510494 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Red/infrared light phototherapy unit 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Red/infrared light phototherapy unit

Boost LED Collar by iSMART Developments, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Red/infrared light phototherapy unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 1967cdd1-8eb1-408c-be05-d6d5b2c6f259 35 fields · synced Jun 1, 2026