PHARMAJET, INC.

FDA Device Registration & Listing · GOLDEN, CO, US · Registration 3004977013

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
3004977013
FEI Number
3004977013
Entity Name
PHARMAJET, INC.
City/State/Country
GOLDEN, CO, US
Establishment Address
400 Corporate Cir Ste N, GOLDEN, CO 80401, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
PHARMAJET, INC. (Owner Number: 9063237)
Owner / Operator Contact Address
400 Corporate Circle, Suite N, Golden, CO 80401, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K111517
PMA Number
N/A

All Registered Proprietary Names

PharmaJet Tropis 0.1ml Needle Free Injection System PharmaJet Stratis Needle-free Injection System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KZE Injector, Fluid, Non-Electrically Powered General Hospital Class 2 880.5430 2018-11-16
KZE Injector, Fluid, Non-Electrically Powered General Hospital Class 2 880.5430 2015-04-02

Official Correspondent

Brent Carpenter

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Similar Registrations

Registration Number Establishment Name Location
3010421104 STERIS TOMOE SINGAPORE PTE LTD Singapore South West, SG
3027739783 RXCROSSROADS 3PL LLC Shepherdsville, KY, US
3008717566 TRIDENT MANUFACTURING, INC. Pingree Grove, IL, US
3012132406 UNIVAC PRECISION ENGINEERING PTE LTD Singapore North West, SG
2027063 NATIONAL MEDICAL PRODUCTS, INC. Irvine, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004977013. Last updated year: 2026. Please use registration number 3004977013 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.