Data / Medical devices / United States / Talbot's Pharmaceuticals Family Products LLC

Talbot's Pharmaceuticals Family Products LLC: FDA-registered device maker in Monroe, LA, United States, 5 510(k) clearances

Name: Talbot's Pharmaceuticals Family Products LLC FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Talbot's Pharmaceuticals Family Products LLC is registered with the FDA (registration 3010822231) in Monroe, LA, United States. It lists 18 device types. The FDA files 5 510(k) clearances under its listings, the newest dated December 18, 2020. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3010822231
Address: 3030 Aurora Ave, 2 FL, Monroe, LA, United States, 71201
Owner or operator: Talbot's Pharmaceuticals Family Products LLC (10054375)
Roles: Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer
First device listed: March 13, 2017
Registered through: 2026
Brand names listed: Dr Talbot's

Devices it lists

Device	Product code	Class	Role	Source
Accessory, Surgical Apparel	LYU	1	Complaint file establishment	accessdata.fda.gov
Catheters, Suction, Tracheobronchial	BSY	1	Complaint file establishment	accessdata.fda.gov
Continuous Measurement Thermometer	FLL	2	Complaint file establishment, Repackager or relabeler	accessdata.fda.gov
Dispenser, Liquid Medication	KYX	1	Complaint file establishment, Specification developer	accessdata.fda.gov
Elastomer, Silicone, For Scar Management	MDA	1	Repackager or relabeler, Specification developer	accessdata.fda.gov
Kit, Test, Pregnancy, Hcg, Over The Counter	LCX	2	Complaint file establishment	accessdata.fda.gov
Massager, Therapeutic, Manual	LYG	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Nebulizer, Medicinal, Non-Ventilatory (Atomizer)	CCQ	1	Repackager or relabeler, Specification developer	accessdata.fda.gov
Nipple, Lambs Feeding	FNN	1	Complaint file establishment, Specification developer	accessdata.fda.gov
Oximeter	DQA	2	Repackager or relabeler	accessdata.fda.gov
Pack, Hot Or Cold, Disposable	IMD	1	Repackager or relabeler, Specification developer	accessdata.fda.gov
Pump, Breast, Non-Powered	HGY	1	Repackager or relabeler	accessdata.fda.gov
Pump, Nebulizer, Electrically Powered	JPW	1	Complaint file establishment, Repackager or relabeler	accessdata.fda.gov
Respirator, Surgical	MSH	2	Complaint file establishment	accessdata.fda.gov
Ring, Teething, Non-Fluid Filled	MEF	1	Complaint file establishment, Repackager or relabeler, Specification developer	accessdata.fda.gov
Syringe, Irrigating (Non Dental)	KYZ	1	Complaint file establishment	accessdata.fda.gov
Toothbrush, Manual	EFW	1	Complaint file establishment, Repackager or relabeler	accessdata.fda.gov
Toothbrush, Powered	JEQ	1	Complaint file establishment	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
December 18, 2020	K201980	Infrared Thermometer	FLL	Substantially Equivalent	Contec Medical Systems Co.,Ltd	accessdata.fda.gov
November 28, 2018	K180207	Non-contact Infrared Thermometer	FLL	Substantially Equivalent	Alicn Medical (Shenzhen), Inc.	accessdata.fda.gov
November 12, 2013	K132085	ONE STEP HCG TEST STRIP, ONE STEP HCG TEST CASSETTE, ONE STEP HCG TEST MIDSTREAM	LCX	Substantially Equivalent	Co-Innovation Biotech Co., Ltd.	accessdata.fda.gov
May 5, 2008	K073454	FINGERTIP PULSE OXIMETER, MODEL CMS-50C	DQA	Substantially Equivalent	Contec Medical System Co., Ltd.	accessdata.fda.gov
November 21, 2002	K023711	DIGITAL THERMOMETER CLASSIC TYPE AND FLEXIBLE TYPE	FLL	Substantially Equivalent	Acute Ideas Co. , Ltd.	accessdata.fda.gov

Compare with other makers

Updated December 18, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.