Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030554525

FEI Number

3030554525

Entity Name

JUBILANT HOLLISTERSTIER LLC

City/State/Country

SPOKANE, WA, US

Establishment Address

3525 N Regal St, SPOKANE, WA 99207, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

JUBILANT HOLLISTERSTIER LLC (Owner Number: 9038322)

Owner / Operator Contact Address

3525 NORTH REGAL ST., --, Spokane, WA 99207, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K953939

PMA Number

N/A

All Registered Proprietary Names

Quintest Skin Test Device Prick Lancetter Quintip Skin Test Device ComforTen Skin Test Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
SCL	Allergen And Vaccine Delivery Needles	General Hospital	Class 2	880.5570	1996-04-08

Official Correspondent

Ben VanGerpen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JUBILANT HOLLISTERSTIER LLC

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
K000299	Biomedex, Inc.	DERMAPIK II SKIN TEST SYSTEM, DERMAPIK II (SINGLE TEST DEVICE), POLYPIK II (MULTIPLE SKIN TEST DEVICE), DERMAPIK TRAY, D	2000-04-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030554525. Last updated year: 2026. Please use registration number 3030554525 when referencing this establishment in official correspondence.