RHONDIUM LIMITED

FDA Device Registration & Listing · Katikati Bay of Plenty, NZ · Registration 3011789026

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
3011789026
FEI Number
3011789026
Entity Name
RHONDIUM LIMITED
City/State/Country
Katikati Bay of Plenty, NZ
Establishment Address
4 Sheffield Street, New Zealand, Katikati Bay of Plenty 3129, NZ
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
RHONDIUM LIMITED (Owner Number: 10049515)
Owner / Operator Contact Address
4 Sheffield Street, New Zealand, Katikati, NZ-BOP 3129, NZ
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Separator Wedge SureMatrix DME Wedge Cementing Wedge Sure Band QuickConnect Anatomy Band Power Ring QuickConnect Carrier R Matrix

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZN Instruments, Dental Hand Dental Class 1 872.4565 2016-12-05
NSM Restoration, Resin Unknown Class N N/A 2024-05-16

Official Correspondent

Greer Fricker

US Agent Details

Floyd Larson Business: PAXMED INTERNATIONAL, LLC Email: flarson@paxmed.com Phone: (858) 7921235

Related Public Records

Same Entity

RHONDIUM LIMITED
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 3011789026. Last updated year: 2026. Please use registration number 3011789026 when referencing this establishment in official correspondence.
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