LASER BIOTECH INTERNATIONAL

FDA Device Registration & Listing · North Chesterfield, VA, US · Registration 3004769071

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004769071
FEI Number
3004769071
Entity Name
LASER BIOTECH INTERNATIONAL
City/State/Country
North Chesterfield, VA, US
Establishment Address
830 Southlake Blvd Ste C, North Chesterfield, VA 23236, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Laser Biotech International (Owner Number: 10060098)
Owner / Operator Contact Address
830 Southlake Blvd., Ste C, Richmond, VA 23236, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Lumix CPS 5 Lumix CPS 2 Lumix CPS 1 Lumix CPS 3 Lumix CPS 4 Lumix Q Lumix CW Lumix Ultra Lumix 3 Plus

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2020-11-10
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2024-06-25
ILY Lamp, Infrared, Therapeutic Heating Physical Medicine Class 2 890.5500 2024-06-25

Official Correspondent

Nelson Marquina

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Laser Biotech International
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004769071. Last updated year: 2026. Please use registration number 3004769071 when referencing this establishment in official correspondence.
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