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Riverpoint Medical LLC

USA · Portland OR · www.rpmed.com

✓ Record-verifiedregistrations found in 12 marketsEU SRN US-MF-000015293

This company has registrations in European Union, United States, United Kingdom, Brazil, Canada, Taiwan, Singapore, South Korea, Australia, Hong Kong, Israel, Russia — 12 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

n/aThis registry lists domestic registrants only

EUEuropean UnionEUDAMED

17UDI-DI device records

Class IIb 17

USUnited StatesFDA openFDA

30listed device types

Class I 8Class II 20Class III 0unclassified 2

plus 72 registration records and 38 510(k)

UKUnited KingdomMHRA PARD

15registered device records

Class I 1Class IIb 8Class III 6

BRBrazilANVISA

1registered devices

Class II 1

3 including historic records

SASaudi ArabiaSFDA

0registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

0active device licences

16 including historic records

TWTaiwanTFDA

6valid device licences

Class I 2Class II 4

SGSingaporeHSA SMDR

3device registrations

CLASS C 3

KRSouth KoreaMFDS GMP

1GMP quality-system certificates

Import 1

AUAustraliaTGA ARTG

21active ARTG entries

Class I 2Class III 2IIa 1IIb 16

HKHong KongMDACS

2valid listings

Class III 1Class IV 1

ILIsraelAMAR

13registrations

RURussiaRoszdravnadzor

1active registrations

Class 2b 1

Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

European Union17 raw hits, 0 excluded, 17 confirmed

United States72 registration records, 38 510(k), 0 PMA

United Kingdom15 confirmed, 0 excluded

Brazil1 confirmed, 0 excluded

Manufacturer names merged into this page: RIVERPOINT MEDICAL LLC · Riverpoint Medical CR S.R.L. · RIVERPOINT MEDICAL · Riverpoint Medical

Regulatory identity

EU manufacturer SRN: US-MF-000015293
EU authorised representative: Emergo Europe B.V.
UK responsible person: Emergo Consulting (UK) Limited

FDA 510(k) clearances by year

12009

22010

12011

12012

12014

22015

22016

12017

12019

22020

12021

82023

92024

42025

22026

FDA listed device types

showing 8 of 30

Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile 1Accelerator, Linear, Medical 1Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile, Exempt 1Marker, Radiographic, Implantable 1Washer, Bolt Nut 1Fastener, Fixation, Biodegradable, Soft Tissue 1Suture, Absorbable, Synthetic, Polyglycolic Acid 1Fastener, Fixation, Nondegradable, Soft Tissue 1

Registration details (sample)

Market	Identifier	Name	Class / date
EU	00812444029864	Iconix® 1	Class IIb
EU	00812444029857	Iconix® 1 TT	Class IIb
EU	00812444029840	Iconix® 1	Class IIb
EU	00840277404763	Iconix® Knotless	Class IIb
UK	33069	Brachytherapy	Class IIb
UK	32037	MedLED Chrome 1.2	Class I
UK	36237	Canalicular Plug	Class IIb
US	K253693	Strut Suture; No-Tie Button	2026-03-11
US	K253695	LigaMend	2026-02-27
US	K253024	ProZip Knotless Implant	2025-10-16
BR	80313660014	CLOTMASTER	Class II