Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1119903

FEI Number

1119903

Entity Name

BTE TECHNOLOGIES

City/State/Country

HANOVER, MD, US

Establishment Address

7455-L NEW RIDGE RD., HANOVER, MD 21076, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

BTE TECHNOLOGIES (Owner Number: 1119903)

Owner / Operator Contact Address

7455-L NEW RIDGE RD., Hanover, MD 21076, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Simulator II SIM II 5 Simulator II SIM II 03 Evaluator Prism Eccentron EvalTech EVJ MCU Multi-Cervical Unit Provider Test Kit (PTK) PrimusRS Alfa

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BXB	Exerciser, Powered	Physical Medicine	Class 1	890.5380	2006-05-09
IKK	System, Isokinetic Testing And Evaluation	Physical Medicine	Class 2	890.1925	2006-05-09
ISD	Exerciser, Measuring	Physical Medicine	Class 2	890.5360	2006-05-09
KHX	Platform, Force-Measuring	Physical Medicine	Class 1	890.1575	2024-02-09

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BTE TECHNOLOGIES

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 1119903. Last updated year: 2026. Please use registration number 1119903 when referencing this establishment in official correspondence.