Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017970304

FEI Number

3017970304

Entity Name

RIM Medical Technologies Incorporated

City/State/Country

Spokane, WA, US

Establishment Address

100 N Howard St., Unit #5439, Spokane, WA 99201, US

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

RIM Medical Technologies Incorporated (Owner Number: 10080310)

Owner / Operator Contact Address

#200, 638 - 11th Ave SW. Calgary, AB, CALGARY, CA-AB T2R 0E2, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Bone Dust Trap

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BYZ	Trap, Sterile Specimen	General Hospital	Class 2	880.6740	2025-01-22

Official Correspondent

Irina Molchanova

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RIM Medical Technologies Incorporated

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 3017970304. Last updated year: 2026. Please use registration number 3017970304 when referencing this establishment in official correspondence.