Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1062154

FEI Number

3000215000

Entity Name

NDH MEDICAL, INC.

City/State/Country

Saint Petersburg, FL, US

Establishment Address

11001 ROOSEVELT BLVD., No. 800, Saint Petersburg, FL 33716, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

NDH MEDICAL, INC. (Owner Number: 9028930)

Owner / Operator Contact Address

11001 ROOSEVELT BLVD., #800, --, St Petersburg, FL 33716, 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
KGZ	Accessories, Catheter	General, Plastic Surgery	Class 1	878.4200	2017-11-29
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2024-04-08
BYY	Tube, Aspirating, Flexible, Connecting	General Hospital	Class 2	880.6740	2018-08-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NDH MEDICAL, 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 1062154. Last updated year: 2026. Please use registration number 1062154 when referencing this establishment in official correspondence.