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Data / Medical devices / United States / Medical Surgical, Inc.

Medical Surgical, Inc.: FDA-registered device maker in Andover, MN, United States, 1 510(k) clearance

Medical Surgical, Inc. is registered with the FDA (registration 2133433) in Andover, MN, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 17, 1995. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2133433
FEI number
1000520823
Address
15596 Avocet St. NW, Andover, MN, United States, 55304
Owner or operator
MEDICAL SURGICAL, INC. (9012475)
Roles
Specification developer
First device listed
February 22, 2008
Registered through
2026
Brand names listed
LIGAMENT SUTURE ANCHORING WASHER

Devices it lists

DeviceProduct codeClassRoleSource
Screw, Fixation, BoneHWC2Specification developeraccessdata.fda.gov
Washer, Bolt NutHTN2Specification developeraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 17, 1995K950250MED-SURG SUTURE WASHERHWCSubstantially Equivalent for Some IndicationsMedical Surgical, Inc.accessdata.fda.gov

Compare with other makers

Updated May 17, 1995. 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.