Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002465911

FEI Number

3002465911

Entity Name

PLANER Limited

City/State/Country

SUNBURY, MIDDLESEX England, GB

Establishment Address

110 WINDMILL ROAD, SUNBURY, MIDDLESEX England TW16 7HD, GB

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Planer Limited (Owner Number: 9054044)

Owner / Operator Contact Address

110 Windmill Road, Sunbury-on-Thames, Middlesex, GB-NOTA TW16 7HD, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BT37 MkII

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PUB	Accessory, Assisted Reproduction, Exempt	Obstetrics/Gynecology	Class 2	884.6120	2017-10-25

Official Correspondent

Nazanin Vahid

US Agent Details

Shawn Riedel Business: Nexpring Health Email: Shawn.riedel@nexpringhealth.com Phone: (303) 5123620

Related Public Records

Same Entity

Planer Limited

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3025301749	TMRW LIFE SCIENCES, Inc.	New York, NY, US
3017838619	WATANABE EQUIPAMENTOS MEDICOS	Cravinhos, Sao Paulo, BR
3009747883	Esco Medical Technologies, UAB	Ramuciai Kauno Apskritis, LT
3007459332	ASTEC CO., Ltd.	Kasuya Fukuoka, JP
3003244268	CRYO BIO SYSTEM	Saint Ouen sur Iton Orne, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002465911. Last updated year: 2026. Please use registration number 3002465911 when referencing this establishment in official correspondence.