PRYOR PRODUCTS

FDA Device Registration & Listing · OCEANSIDE, CA, US · Registration 2023337

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
2023337
FEI Number
2023337
Entity Name
PRYOR PRODUCTS
City/State/Country
OCEANSIDE, CA, US
Establishment Address
1819 PEACOCK BLVD., OCEANSIDE, CA 92056, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
PRYOR PRODUCTS (Owner Number: 2023337)
Owner / Operator Contact Address
1819 PEACOCK BLVD., --, Oceanside, CA 92056, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PATIENT PAL ATLAS HANGER WHEELCHAIR PAL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FOX Stand, Infusion General Hospital Class 1 880.6990 1992-11-19
KNO Accessories, Wheelchair Physical Medicine Class 1 890.3910 1992-11-19
JAY Support, Breathing Tube Anesthesiology Class 1 868.5280 2024-05-09
BRY Cabinet, Table And Tray, Anesthesia Anesthesiology Class 1 868.6100 2024-05-09

Official Correspondent

JEFF PRYOR

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PRYOR PRODUCTS
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2023337. Last updated year: 2026. Please use registration number 2023337 when referencing this establishment in official correspondence.
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