STEREX ELECTROLYSIS INTL., LTD.

FDA Device Registration & Listing · BIRMINGHAM, GB · Registration 9681366

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
9681366
FEI Number
1000439607
Entity Name
STEREX ELECTROLYSIS INTL., LTD.
City/State/Country
BIRMINGHAM, GB
Establishment Address
174 KINGS RD.,, TYSELEY, BIRMINGHAM B11 2AP, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
STEREX ELECTROLYSIS INTL., LTD. (Owner Number: 9022281)
Owner / Operator Contact Address
174 KINGS RD.,, TYSELEY, BIRMINGHAM, GB-NOTA B11 2AP, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

sterex

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KCW Epilator, High Frequency, Needle-Type General, Plastic Surgery Class 1 878.5350 2007-11-30

Official Correspondent

Christopher CARTMELL

US Agent Details

Susan Poczobut Email: spoczobut@gmail.com Phone: (802) 7938191

Related Public Records

Same Entity

STEREX ELECTROLYSIS INTL., LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K954031 R. A. Fischer Co. Corp. COMPU-BLEND EPILATOR 1996-01-05

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9681366. Last updated year: 2026. Please use registration number 9681366 when referencing this establishment in official correspondence.
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