Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010886592

FEI Number

3010886592

Entity Name

Rush Order

City/State/Country

Gilroy, CA, US

Establishment Address

6205 Engle Way, Suite A, Gilroy, CA 95020, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Rush Order (Owner Number: 10088466)

Owner / Operator Contact Address

6600 Silacci Way, Gilroy, CA 95020, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

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	2023-07-27

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Rush Order

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 3010886592. Last updated year: 2026. Please use registration number 3010886592 when referencing this establishment in official correspondence.