Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010759902

FEI Number

3010759902

Entity Name

Alphapointe

City/State/Country

Jamaica, NY, US

Establishment Address

87-46 123rd street, Jamaica, NY 11418, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Alphapointe (Owner Number: 10046233)

Owner / Operator Contact Address

7501 Prospect, Kansas City, MO 64132, 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
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2014-02-20
MHW	Dressing, Compression	General Hospital	Class 1	880.5075	2021-12-07
KCY	Tourniquet, Pneumatic	General, Plastic Surgery	Class 1	878.5910	2014-02-20

Official Correspondent

Staci Jackson-Weir

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Alphapointe

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1932015	ALPHAPOINTE	KANSAS CITY, MO, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010759902. Last updated year: 2026. Please use registration number 3010759902 when referencing this establishment in official correspondence.