Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1932015

FEI Number

1000118260

Entity Name

ALPHAPOINTE

City/State/Country

KANSAS CITY, MO, US

Establishment Address

7501 PROSPECT AVE, KANSAS CITY, MO 64132, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Alphapointe (Owner Number: 9002620)

Owner / Operator Contact Address

7501 PROSPECT AVE., --, 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

Alpha Cravat Walking heel RISE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ILI	Sling, Arm	Physical Medicine	Class 1	890.3640	2025-02-10
LGF	Component, Cast	Orthopedic	Class 1	888.5940	2013-09-06
NOC	Splint, Extremity, Non-Inflatable, External, Non-Sterile	General, Plastic Surgery	Class 1	878.3910	2013-09-06
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2023-05-19

Official Correspondent

Amy McCaslin

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
3010759902	Alphapointe	Jamaica, NY, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1932015. Last updated year: 2026. Please use registration number 1932015 when referencing this establishment in official correspondence.