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Terrats Medical, S.L.: FDA-registered device maker in Barbera del Valles Barcelona, Spain, 23 510(k) clearances

Terrats Medical, S.L. is registered with the FDA (registration 3014118611) in Barbera del Valles Barcelona, Spain. It lists 4 device types. The FDA files 23 510(k) clearances under its listings, the newest dated June 9, 2026. Registered through 2027. FDA data exported November 3, 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.

FDA registration number
3014118611
Address
Mogoda, 75, Barbera del Valles Barcelona, Spain, 08210
Owner or operator
Terrats Medical, S.L. (10056484)
Roles
Contract manufacturer, Manufacturer
First device listed
December 14, 2017
Registered through
2027
Brand names listed
Argen, DESS Dental Smart Solutions, DIRECTarch, INTEGRATED DENTAL SYSTEMS, TERRATS MEDICAL, S.L., Terrats Medical S.L.

Devices it lists

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 9, 2026K260564DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
April 16, 2026K253804DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
October 31, 2025K251547DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
October 23, 2025K252384DESS® Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
July 23, 2025K251280DESS® Dental ImplantsDZESubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
May 22, 2025K250639DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
February 14, 2025K243212DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
November 5, 2024K242340DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
August 26, 2024K240982DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
April 24, 2024K240208DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
January 5, 2024K233316DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
August 14, 2023K231434DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
April 13, 2023K230143DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
March 9, 2023K221301DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
October 27, 2022K222288DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
October 26, 2022K222269DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
March 11, 2022K212628DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
December 14, 2021K212538DESS Dental ImplantsDZESubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
December 10, 2021K212577DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
August 4, 2021K203464DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
November 10, 2019K191986DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
June 15, 2018K173908DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov
August 8, 2017K170588DESS Dental Smart SolutionsNHASubstantially EquivalentTerrats Medical SLaccessdata.fda.gov

Compare with other makers

Updated June 9, 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.