Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006791549

FEI Number

3006791549

Entity Name

Lab Warehouse Inc.

City/State/Country

Lajas, PR, US

Establishment Address

Carr. 116 Km 8.6, Bo.Costas, Lajas, PR 00667, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Lab Warehouse Inc. (Owner Number: 10022961)

Owner / Operator Contact Address

Bo Costas Carr. 116 Km. 8.6, Lajas, PR 00667, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GGK	Products, Red-Cell Lysing Products	Hematology	Class 1	864.8540	2025-01-17
PPM	General Purpose Reagent	Pathology	Class 1	864.4010	2025-01-17
GIF	Diluent, Blood Cell	Hematology	Class 1	864.8200	2025-01-17

Official Correspondent

Jose Sanchez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lab Warehouse Inc.

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 3006791549. Last updated year: 2026. Please use registration number 3006791549 when referencing this establishment in official correspondence.