FFA, LLC div Prostat First Aid

FDA Device Registration & Listing · La Verne, CA, US · Registration 3010934856

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3010934856
FEI Number
3010934856
Entity Name
FFA, LLC div Prostat First Aid
City/State/Country
La Verne, CA, US
Establishment Address
1643 Puddingstone Drive, La Verne, CA 91750, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
FFA, LLC DBA Prostat First Aid (Owner Number: 10046938)
Owner / Operator Contact Address
24922 Anza Dr Unit A, Valencia, CA 91355, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Prostat ProStat ProStat Prostat Front Line Prostat Prostat Front Line

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQM Bandage, Elastic General Hospital Class 1 880.5075 2015-11-05
CBP Valve, Non-Rebreathing Anesthesiology Class 2 868.5870 2023-05-29
KME Bedding, Disposable, Medical General Hospital Class 1 880.6060 2025-06-12
FRL Fiber, Medical, Absorbent General Hospital Class 1 880.5300 2015-11-05
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2015-11-05
OVR Kit, First Aid, Talking General, Plastic Surgery Class 1 878.4014 2022-10-27
IMD Pack, Hot Or Cold, Disposable Physical Medicine Class 1 890.5710 2016-01-14
FME Gown, Examination General Hospital Class 1 880.6265 2022-10-28
LZB Finger Cot General Hospital Class 1 880.6250 2021-05-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FFA, LLC DBA Prostat First Aid
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
K945177 Eagle Health Supplies 4-O2 JR. (CPR MOUTH BARRIER) 1994-11-01
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010934856. Last updated year: 2026. Please use registration number 3010934856 when referencing this establishment in official correspondence.
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