Howard Wright Limited

FDA Device Registration & Listing · New Plymouth Taranaki, NZ · Registration 1000211739

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
1000211739
FEI Number
1000211739
Entity Name
Howard Wright Limited
City/State/Country
New Plymouth Taranaki, NZ
Establishment Address
Paraite Road, Bell Block, New Plymouth Taranaki 4373, NZ
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Howard Wright Limited (Owner Number: 10021845)
Owner / Operator Contact Address
Paraite Road, Bell Block, New Plymouth, NZ-TKI 4373, NZ
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

M9 Trauma and Transfer Stretcher Range Pacific Shower-Bathing Trolley

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FPO Stretcher, Wheeled General Hospital Class 2 880.6910 2019-03-21
FSA Lift, Patient, Non-Ac-Powered General Hospital Class 1 880.5510 2014-12-11

Official Correspondent

Bruce Moller

US Agent Details

Michael Joswick Business: T.F. HERCEG, INC. Email: joswick@surehands.com Phone: (781) 6407904

Related Public Records

Same Entity

Howard Wright Limited
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0023-05 Stryker Medical 2
Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.
Z-0013-2018 Handicare Usa Inc 1
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018 Handicare AB Maskinvagen 1
Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000211739. Last updated year: 2026. Please use registration number 1000211739 when referencing this establishment in official correspondence.
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