Data / Medical devices / United States / FFA, LLC div Prostat First Aid

FFA, LLC div Prostat First Aid: FDA-registered device maker in La Verne, CA, United States, 1 510(k) clearance

Name: FFA, LLC div Prostat First Aid FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

FFA, LLC div Prostat First Aid is registered with the FDA (registration 3010934856) in La Verne, CA, United States. It lists 13 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 22, 2010. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 3010934856
Address: 1643 Puddingstone Drive, La Verne, CA, United States, 91750
Owner or operator: FFA, LLC DBA Prostat First Aid (10046938)
Roles: Repackager or relabeler
First device listed: November 5, 2015
Registered through: 2027
Brand names listed: Front Line, ProStat, Prostat

Devices it lists

Device	Product code	Class	Role	Source
Applicator, Absorbent Tipped, Non-Sterile	KXF	1	Repackager or relabeler	accessdata.fda.gov
Bandage, Elastic	FQM	1	Repackager or relabeler	accessdata.fda.gov
Bedding, Disposable, Medical	KME	1	Repackager or relabeler	accessdata.fda.gov
Dressing, Wound, Hydrogel Without Drug And/Or Biologic	NAE	1	Repackager or relabeler	accessdata.fda.gov
Fiber, Medical, Absorbent	FRL	1	Repackager or relabeler	accessdata.fda.gov
Finger Cot	LZB	1	Repackager or relabeler	accessdata.fda.gov
Gauze / Sponge,Nonresorbable For External Use	NAB	1	Repackager or relabeler	accessdata.fda.gov
Gown, Examination	FME	1	Repackager or relabeler	accessdata.fda.gov
Kit, First Aid, Talking	OVR	1	Repackager or relabeler	accessdata.fda.gov
Pack, Hot Or Cold, Disposable	IMD	1	Repackager or relabeler	accessdata.fda.gov
Splint, Extremity, Non-Inflatable, External, Non-Sterile	NOC	1	Repackager or relabeler	accessdata.fda.gov
Tape And Bandage, Adhesive	KGX	1	Repackager or relabeler	accessdata.fda.gov
Valve, Non-Rebreathing	CBP	2	Repackager or relabeler	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
July 22, 2010	K083418	CPR MASK	CBP	Substantially Equivalent	Firstar Healthcare Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated July 22, 2010. 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.