← Back to catalogue

Lightforce

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
LIGHTFORCE FDA UDI
Generic Name
Musculoskeletal/physical therapy laser beam guide, transcutaneous FDA UDI
Device Name
Trade-In 800um SHP v2 Assy LightForce - more than 5 yrs old FDA UDI
Model / Reference
PRD-000758-010-00-L-G5 FDA UDI
Description
Trade-In 800um SHP v2 Assy LightForce - more than 5 yrs old FDA UDI

Identifiers

Primary DI / UDI-DI
00190446897903 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Musculoskeletal/physical therapy laser beam guide, transcutaneous 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Musculoskeletal/physical therapy laser beam guide, transcutaneous

Lightforce by Djo, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Musculoskeletal/physical therapy laser beam guide, transcutaneous.

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

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 93757623-8a46-4c73-8397-6cd52989dd7d 33 fields · synced May 30, 2026