Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012782440

FEI Number

3012782440

Entity Name

KASM INTERNATIONAL LLC

City/State/Country

Orlando, FL, US

Establishment Address

20 North Orange Ave, Suite 1107, Orlando, FL 32801, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

KASM International LLC (Owner Number: 10052767)

Owner / Operator Contact Address

20 North Orange Ave, Suite 1107, Orlando, FL 32801, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TrekProof

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IME	Pack, Hot Or Cold, Reusable	Physical Medicine	Class 1	890.5700	2022-04-14

Official Correspondent

Kyle Morrison

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KASM International LLC

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 3012782440. Last updated year: 2026. Please use registration number 3012782440 when referencing this establishment in official correspondence.