Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9680836

FEI Number

3005892511

Entity Name

BIO NUCLEAR DIAGNOSTICS, INC.

City/State/Country

TORONTO Ontario, CA

Establishment Address

1791 ALBION RD., TORONTO Ontario M9W 5S7, CA

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

BIO NUCLEAR DIAGNOSTICS, INC. (Owner Number: 9008756)

Owner / Operator Contact Address

1791 ALBION RD., --, TORONTO, ONTARIO, CA-NOTA M9W 5S7, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Technologist Choice Transfer Pipette Transfer Pipette Technologist Choice urine cups Urine Collection container - Saturo Technologist Choice Fecal Wooden Applicator Applicator, non-sterile, cotton tip, 6" Technologist Choice Applicator, non-sterile, cotton tip, 6" TECHNOLOGIST CHOICE TOURNIQUET

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JRC	Micro Pipette	Clinical Chemistry	Class 1	862.2050	2001-05-30
NNI	Container, Specimen, Non-Sterile	Pathology	Class 1	864.3250	2017-03-22
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	1994-01-04
JRQ	Shaker/Stirrer	Clinical Chemistry	Class 1	862.2050	2018-04-09
KXF	Applicator, Absorbent Tipped, Non-Sterile	General Hospital	Class 1	880.6025	2017-03-28
GAX	Tourniquet, Nonpneumatic	General, Plastic Surgery	Class 1	878.5900	2019-07-23

Official Correspondent

RAVI KIRAN CHOUDHRY

US Agent Details

Conor OMalley Email: conorjomalley@gmail.com Phone: (847) 8097010

Related Public Records

Same Entity

BIO NUCLEAR DIAGNOSTICS, INC.

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 9680836. Last updated year: 2026. Please use registration number 9680836 when referencing this establishment in official correspondence.