Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2030580

FEI Number

1000518699

Entity Name

Tulip Medical Products, Inc.

City/State/Country

San Diego, CA, US

Establishment Address

4360 Morena Blvd Ste 100, San Diego, CA 92117, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Tulip Medical Products Inc., (Owner Number: 10028110)

Owner / Operator Contact Address

4360 Morena Blvd, Suite 100, San Diego, CA 92117, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tulip Medical Products

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GDM	Needle, Aspiration And Injection, Reusable	General, Plastic Surgery	Class 1	878.4800	2008-12-30

Official Correspondent

Marcille Pilkington

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tulip Medical Products Inc.,

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2030580. Last updated year: 2026. Please use registration number 2030580 when referencing this establishment in official correspondence.