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Sic Invent AG: FDA-registered device maker in Basel Town Basel-Landschaft, Switzerland, 7 510(k) clearances

Name: Sic Invent AG FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Sic Invent AG is registered with the FDA (registration 3004443656) in Basel Town Basel-Landschaft, Switzerland. It lists 5 device types. The FDA files 7 510(k) clearances under its listings, the newest dated June 3, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3004443656
Address: Birmannsgasse 3, Basel Town Basel-Landschaft, Switzerland, 4055
Owner or operator: SIC invent AG (9060857)
Roles: Exporter to the US, Manufacturer
First device listed: May 26, 2005
Registered through: 2026
Brand names listed: 951378, 951416, 951417, 951422, 951423, 951424, 951425, 951426 and more

Devices it lists

Device	Product code	Class	Role	Source
Abutment, Implant, Dental, Endosseous	NHA	2	Exporter to the US, Manufacturer	accessdata.fda.gov
Accessories, Implant, Dental, Endosseous	NDP	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Dental Implant Surgical Tray	OFY	1	Manufacturer	accessdata.fda.gov
Handpiece, Direct Drive, Ac-Powered	EKX	1	Exporter to the US	accessdata.fda.gov
Implant, Endosseous, Root-Form	DZE	2	Exporter to the US, 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
June 3, 2026	K252904	SIC Abutments including CAD/CAM Solutions	NHA	Substantially Equivalent	Sic Invent AG	accessdata.fda.gov
March 17, 2022	K210489	SICtapered & SICvantage tapered	DZE	Substantially Equivalent	Sic Invent AG	accessdata.fda.gov
November 16, 2018	K180184	Zeramex(R) XT Dental Implant System, NobelPearl Dental Implant System	NHA	Substantially Equivalent	Dentalpoint AG	accessdata.fda.gov
April 5, 2018	K173207	SIC invent Dental Implant Systems	DZE	Substantially Equivalent	Sic Invent AG	accessdata.fda.gov
January 7, 2016	K143445	Tellos ISQ Buddy	EKX	Substantially Equivalent	Tellos Medical AB	accessdata.fda.gov
December 3, 2007	K072878	MODIFICATION TO: LOCATOR IMPLANT ANCHOR	NHA	Substantially Equivalent	Zest Anchors, Inc.	accessdata.fda.gov
March 17, 2000	K994257	LOCATOR IMPLANT ANCHOR	DZE	Substantially Equivalent	Zest Anchors, Inc.	accessdata.fda.gov

Compare with other makers

Updated June 3, 2026. 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.