PRIDE Industries

FDA Device Registration & Listing · Roseville, CA, US · Registration 3008570882

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
3008570882
FEI Number
2937446
Entity Name
PRIDE Industries
City/State/Country
Roseville, CA, US
Establishment Address
10030 Foothills Blvd, Roseville, CA 95747, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
PRIDE Industries (Owner Number: 10042055)
Owner / Operator Contact Address
10030 Foothills Blvd., Roseville, CA 95747, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CORTRAK* 2 Enteral Access System Game Ready Therapy System Med4 Elite Game Ready System Versa Pump Immunoglobulin G (Igg) Infusion System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNT Tubes, Gastrointestinal (And Accessories) Gastroenterology, Urology Class 2 876.5980 2025-12-30
ILO Pack, Hot Or Cold, Water Circulating Physical Medicine Class 2 890.5720 2012-10-11
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2012-10-11
ILO Pack, Hot Or Cold, Water Circulating Physical Medicine Class 2 890.5720 2022-03-01
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2022-03-01
ILO Pack, Hot Or Cold, Water Circulating Physical Medicine Class 2 890.5720 2020-06-02
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2020-06-02
PKP Immunoglobulin G (Igg) Infusion System General Hospital Class 2 880.5725 2026-04-30

Official Correspondent

Brittney Blue

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PRIDE Industries
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
K900590 Biosearch Medical Products, Inc. BIOSEARCH DOBBHOFF(R) GASTROTRAC JEJUNAL FEEDING 1990-08-02
K102548 Footprint Medical, Inc. FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE 2010-11-26
K955248 United States Endoscopy Group, Inc. U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT 1996-05-21
K872921 Medical Support, Inc. MSS ENTERAL DELIVERY SET 1987-12-03
K180622 Covidien Kangaroo Gastrostomy Feeding Tube with ENFit Y-Port 2018-10-23

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3009247326 Jabil Circuit (Singapore) Pte Ltd Singapore Central Singapore, SG
2528981 LYNX Medical Pennsylvania ERIE, PA, US
1649518 Sterigenics US LLC Fort Worth, TX, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008570882. Last updated year: 2026. Please use registration number 3008570882 when referencing this establishment in official correspondence.
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