Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2087341

FEI Number

3003532699

Entity Name

GIBBONS HEALTH PRODUCTS, INC.

City/State/Country

STUDIO CITY, CA, US

Establishment Address

11333 MOORPARK ST., No. 424, STUDIO CITY, CA 91602, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

GIBBONS HEALTH PRODUCTS, INC. (Owner Number: 9048869)

Owner / Operator Contact Address

1534 Moorpark Rd, 350, Thousand Oaks, CA 91360, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dr. Bob's Health Products Inc. Dr. Bob's

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HST	Apparatus, Traction, Non-Powered	Orthopedic	Class 1	888.5850	2016-07-05

Official Correspondent

ROBERT GIBBONS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GIBBONS HEALTH PRODUCTS, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3004012851	IHN, INC	Okemos, MI, US
3023187489	MAGNATE HEALTH TECH. CO., LTD	TAIPEI CITY, TW
3014680784	Domico Med-Device, LLC	Fenton, MI, US
2936485	STRYKER ENDOSCOPY	SAN JOSE, CA, US
3011219098	MFG AMP	Tijuana Baja California, MX

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2087341. Last updated year: 2026. Please use registration number 2087341 when referencing this establishment in official correspondence.