PRESSURE PRODUCTS, INC.

FDA Device Registration & Listing · Santa Barbara, CA, US · Registration 2025881

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
2025881
FEI Number
2025881
Entity Name
PRESSURE PRODUCTS, INC.
City/State/Country
Santa Barbara, CA, US
Establishment Address
49 Via Alicia, Santa Barbara, CA 93108, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
PRESSURE PRODUCTS MEDICAL SUPPLIES, INC. (Owner Number: 2025881)
Owner / Operator Contact Address
49 Via Alicia, --, Santa Barbara, CA 93108, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HOLD DEVICE POCKET PAL HEMOBILIZER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQM Bandage, Elastic General Hospital Class 1 880.5075 1992-11-17
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 1992-11-17

Official Correspondent

PAUL KURTH

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PRESSURE PRODUCTS MEDICAL SUPPLIES, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2025881. Last updated year: 2026. Please use registration number 2025881 when referencing this establishment in official correspondence.
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