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Empower Delivery System

FDA UDI

Class II (US FDA UDI)

by Litecure Llc

Identity

Trade Name
Empower Delivery System FDA UDI
Generic Name
Musculoskeletal/physical therapy laser beam guide, transcutaneous FDA UDI
Device Name
Legacy Hand Piece 800um Fiber Hand Piece w/ Finger Switch, Cool Gray FDA UDI
Model / Reference
PRD-000477-000-01-L FDA UDI
Description
Legacy Hand Piece 800um Fiber Hand Piece w/ Finger Switch, Cool Gray FDA UDI

Identifiers

Primary DI / UDI-DI
00854103007165 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

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

Yes

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

Empower Delivery System by Litecure 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

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Manufacturer

Manufacturer
Litecure Llc

Sources (1)

  • FDA UDI 0e6cb90e-294a-4970-9a3c-43cee13e068f 33 fields · synced Jun 8, 2026