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Data / Medical devices / Netherlands / TSC Life

TSC Life: FDA-registered device maker in Almelo Overijssel, Netherlands, 5 510(k) clearances

TSC Life is registered with the FDA (registration 3021073836) in Almelo Overijssel, Netherlands. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated August 7, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3021073836
Address
Bedrijvenpark Twente Noord 48 --, Almelo Overijssel, Netherlands, 7602 KR
Owner or operator
THE SURGICAL COMPANY INTERNATIONAL BV (9101201)
Roles
Manufacturer
First device listed
July 8, 2010
Registered through
2026
Brand names listed
Fluido Compact Control Module, Fluido Compact Standard Set, Fluido Compact Standard Set with Drip Chamber, Fluido Compact Warming Module, Fluido® AirGuard, Fluido® Blood & Fluid Warmer (115V), Fluido® Compact Holder, Fluido® Compressor and more

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
August 7, 2026K261437Mistral-Air® Warming SystemDWJSubstantially EquivalentThe Surgical Company International B.V., doing business as TSC Lifeaccessdata.fda.gov
November 18, 2025K252636Fluido Compact SystemLGZSubstantially EquivalentThe Surgical Company International B.V.accessdata.fda.gov
September 4, 2025K251733Fluido® AirGuard SystemLGZSubstantially EquivalentThe Surgical Company International BV (As Tsc Life)accessdata.fda.gov
May 26, 2017K171234Mistral-Air Warming UnitDWJSubstantially EquivalentThe Surgical Company International BV (As the 37company)accessdata.fda.gov
July 2, 2010K101705MISTRAL-AIR WARMING SYSTEMDWJSubstantially EquivalentThe Surgical Company International B.V.accessdata.fda.gov

Compare with other makers

Updated August 7, 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.