Data / Medical devices / Costa Rica / Riverpoint Medical CR S.R.L.

Riverpoint Medical CR S.R.L.: FDA-registered device maker in Coyol Alajuela, Costa Rica, 9 510(k) clearances

Name: Riverpoint Medical CR S.R.L. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Riverpoint Medical CR S.R.L. is registered with the FDA (registration 3027454646) in Coyol Alajuela, Costa Rica. It lists 4 device types. The FDA files 9 510(k) clearances under its listings, the newest dated July 30, 2025. Registered through 2027. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch Riverpoint Medical CR S.R.L.

FDA registration number: 3027454646
Address: Coyol Free Zone Building 3A, Coyol Alajuela, Costa Rica, 20113
Owner or operator: Riverpoint Medical LLC (10024181)
Roles: Contract manufacturer, Manufacturer
First device listed: December 8, 2020
Registered through: 2027
Brand names listed: CHROMIC GUT; PLAIN GUT, CP COTTON UMBILICAL TAPE, OrthoButton AL, OrthoButton FL

Devices it lists

Device	Product code	Class	Role	Source
Fastener, Fixation, Nondegradable, Soft Tissue	MBI	2	Manufacturer	accessdata.fda.gov
Suture, Absorbable, Natural	GAL	2	Contract manufacturer	accessdata.fda.gov
Suture, Nonabsorbable, Synthetic, Polyethylene	GAT	2	Manufacturer	accessdata.fda.gov
Truss, Umbilical	EXM	1	Contract manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
July 30, 2025	K252144	Iconix Speed Anchor; Iconix Speed HA+ Anchor	MBI	Substantially Equivalent	Riverpoint Medical	accessdata.fda.gov
November 19, 2024	K243323	Iconix Knotless Anchor	MBI	Substantially Equivalent	Riverpoint Medical	accessdata.fda.gov
February 23, 2024	K240213	Iconix Knotless Anchor	MBI	Substantially Equivalent	Riverpoint Medical	accessdata.fda.gov
August 1, 2023	K231278	Knotless Suture Anchor	MBI	Substantially Equivalent	Riverpoint Medical, LLC	accessdata.fda.gov
May 17, 2023	K231128	JuggerKnot Soft Anchor	MBI	Substantially Equivalent	Riverpoint Medical, LLC	accessdata.fda.gov
February 23, 2023	K230212	OrthoButton AL	MBI	Substantially Equivalent	Riverpoint Medical, LLC	accessdata.fda.gov
February 12, 2021	K203740	JuggerKnot Soft Anchor	MBI	Substantially Equivalent	Riverpoint Medical	accessdata.fda.gov
September 18, 2020	K202399	OrthoButton FL	MBI	Substantially Equivalent	Riverpoint Medical	accessdata.fda.gov
September 10, 2020	K202242	HS Fiber	GAT	Substantially Equivalent	Riverpoint Medical, LLC	accessdata.fda.gov

Compare with other makers

Updated July 30, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.