Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007485597

FEI Number

3007485597

Entity Name

CAMNTECH

City/State/Country

Fenstanton Cambridgeshire, GB

Establishment Address

Manor Farm, Fenstanton Cambridgeshire PE289JD, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CamNtech (Owner Number: 10028414)

Owner / Operator Contact Address

Manor Farm, Fenstanton, GB-CAM PE289JD, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K132764

PMA Number

N/A

All Registered Proprietary Names

MotionWatch 8 MotionWatch PRO-Diary

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LEL	Device, Sleep Assessment	Neurology	Class 2	882.5050	2014-07-17

Official Correspondent

Howard Smith

US Agent Details

Dennis McCarthy Business: CamNtech Inc Email: dennismccarthy@camntech.com Phone: (830) 7558075

Related Public Records

Same Entity

CamNtech

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 3007485597. Last updated year: 2026. Please use registration number 3007485597 when referencing this establishment in official correspondence.