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Lzr7

FDA UDI

Class II (US FDA UDI)

by Lzr7, Inc.

Identity

Trade Name
LZR7 FDA UDI
Generic Name
Musculoskeletal/physical therapy laser, home-use FDA UDI
Device Name
Pro3M Laser Unit FDA UDI
Model / Reference
Pro3M FDA UDI
Description
Pro3M Laser Unit FDA UDI

Identifiers

Primary DI / UDI-DI
B657002 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Musculoskeletal/physical therapy laser, home-use 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

Yes

FDA UDI

Category: Musculoskeletal/physical therapy laser, home-use

Lzr7 by Lzr7, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Musculoskeletal/physical therapy laser, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lzr7, Inc.

Sources (1)

  • FDA UDI 3eed4749-fbb4-445e-9ed9-2c0b689b6af3 33 fields · synced Jun 8, 2026