Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010822231

FEI Number

3010822231

Entity Name

TALBOT'S PHARMACEUTICALS FAMILY PRODUCTS LLC

City/State/Country

Monroe, LA, US

Establishment Address

3030 Aurora Ave, 2 FL, Monroe, LA 71201, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Talbot's Pharmaceuticals Family Products LLC (Owner Number: 10054375)

Owner / Operator Contact Address

3030 Aurora Ave, 2 FL, Monroe, LA 71201, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dr Talbot's

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LYU	Accessory, Surgical Apparel	General, Plastic Surgery	Class 1	878.4040	2020-04-07
FNN	Nipple, Lambs Feeding	General Hospital	Class 1	880.5640	2020-07-14
EFW	Toothbrush, Manual	Dental	Class 1	872.6855	2017-03-13
LYG	Massager, Therapeutic, Manual	Physical Medicine	Class 1	890.5660	2025-07-18
IMD	Pack, Hot Or Cold, Disposable	Physical Medicine	Class 1	890.5710	2023-10-20
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2022-05-20
JPW	Pump, Nebulizer, Electrically Powered	Ear, Nose, Throat	Class 1	874.5220	2022-11-15
MDA	Elastomer, Silicone, For Scar Management	General, Plastic Surgery	Class 1	878.4025	2023-10-20
CCQ	Nebulizer, Medicinal, Non-Ventilatory (Atomizer)	Anesthesiology	Class 1	868.5640	2023-10-20
MSH	Respirator, Surgical	General, Plastic Surgery	Class 2	878.4040	2020-04-07
JEQ	Toothbrush, Powered	Dental	Class 1	872.6865	2020-05-25
KYZ	Syringe, Irrigating (Non Dental)	General Hospital	Class 1	880.6960	2021-11-18
LCX	Kit, Test, Pregnancy, Hcg, Over The Counter	Clinical Chemistry	Class 2	862.1155	2020-11-05
KYX	Dispenser, Liquid Medication	General Hospital	Class 1	880.6430	2019-06-06

Official Correspondent

Joseph Hakim

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Talbot's Pharmaceuticals Family Products LLC

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
K973236	Procter & Gamble Co.	CREST TOOTHBRUSH WITH MICROSHIELD	1998-03-11
K880871	John Wagner Associates, Inc.	GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER	1988-05-20
K102092	Prestige Ameritech	PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES	2010-10-06
K964108	Direct Access Diagnostics	FACT PLUS PREGNANCY TEST	1996-11-18
K945514	Princeton BioMeditech Corp.	LIFESIGN(TM) 1, BIOSIGN(TM) 1, LIFESIGN PLUS(TM), LIFESIGN(TM) HCG	1995-02-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0505-2022	Philips North America Llc	1	Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022	Philips North America Llc	1	Infant Heel Warmers w/strap, Reference # 989805603201 1223
Z-0042-2024	Universal Meditech Inc.	2	One Step Pregnancy Test REF 100-01

Similar Registrations

Registration Number	Establishment Name	Location
9680454	EMPRESAS IAI S DE RL DE C.V.	H. MATAMOROS Tamaulipas, MX
3010227982	Tianjin Zhengtian Medical Instrument Co., Ltd.	Tianjin, CN
3016871880	PRIMEX DESIGN & FABRICATION	Richmond, IN, US
3005360866	QEL DOMINICANA S.A.	ESPERANZA Valverde, DO
3010601984	Jiangsu Haize Medical Scientific Development Co.,Ltd.	Wuxi Jiangsu, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010822231. Last updated year: 2026. Please use registration number 3010822231 when referencing this establishment in official correspondence.