PatchRx, Inc.

FDA Device Registration & Listing · Wilmington, DE, US · Registration 3025662433

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
3025662433
FEI Number
3025662433
Entity Name
PatchRx, Inc.
City/State/Country
Wilmington, DE, US
Establishment Address
800 N King St Ste 304 # 2867, Wilmington, DE 19801, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Patch Technologies, Inc. (Owner Number: 10084551)
Owner / Operator Contact Address
100 S Cincinnati Ave, Ste 504, Tulsa, OK 74103, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PatchCap

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NXB Dispenser, Solid Medication Physical Medicine Class 1 890.5050 2022-12-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Patch Technologies, Inc.
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
K944481 Garan Scientific, Inc. THE HEART PROTECTOR 1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3025662433. Last updated year: 2026. Please use registration number 3025662433 when referencing this establishment in official correspondence.
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