Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000587715

FEI Number

1000125602

Entity Name

BLUE POPPY ENTERPRISES

City/State/Country

Portland, OR, US

Establishment Address

4804 SE 69TH AVE, Portland, OR 97206, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Blue Poppy Enterprises (Owner Number: 10072710)

Owner / Operator Contact Address

4804 SE 69TH AVE, Portland, OR 97206, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K150903

PMA Number

N/A

All Registered Proprietary Names

BALANCE TEMPO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQX	Needle, Acupuncture, Single Use	General Hospital	Class 2	880.5580	2020-04-30

Official Correspondent

Pei Li

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Blue Poppy Enterprises

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 1000587715. Last updated year: 2026. Please use registration number 1000587715 when referencing this establishment in official correspondence.