Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014562978

FEI Number

3014562978

Entity Name

C.G. Laboratories-Bob White

City/State/Country

Granbury, TX, US

Establishment Address

2449 Bob White Dr., Granbury, TX 76049, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

C.G. LABORATORIES, INC. (Owner Number: 9031587)

Owner / Operator Contact Address

1410 SOUTHTOWN DR., --, Granbury, TX 76048, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

N-TERFACE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MGP	Dressing, Wound And Burn, Occlusive	Unknown	Class U	N/A	2012-11-07

Official Correspondent

RUSSELL CRUM

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

C.G. LABORATORIES, INC.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K953018	Ttl Medical	UNI-SITE	1995-09-08

Similar Registrations

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3010041511	Teleflex LLC (NADC)	Olive Branch, MS, US
3005012805	MIDWEST STERILIZATION CORP.	LAREDO, TX, US
1644312	MedXL	ARDMORE, OK, US
3010034780	Smith & Nephew, Inc.	Lawrenceville, GA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014562978. Last updated year: 2026. Please use registration number 3014562978 when referencing this establishment in official correspondence.