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Data / Medical devices / United States / Medtec Applications, Inc.

Medtec Applications, Inc.: FDA-registered device maker in Glendale Heights, IL, United States, 2 510(k) clearances

Medtec Applications, Inc. is registered with the FDA (registration 1483278) in Glendale Heights, IL, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 1, 1996. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1483278
Address
35 N Brandon Dr, Glendale Heights, IL, United States, 60139
Owner or operator
MEDTEC APPLICATIONS, INC. (1483278)
Roles
Manufacturer
First device listed
July 27, 1992
Registered through
2026
Brand names listed
ARTHROSCOPE, GYNECOLOGIC (AND ACCESSORIES), LAPAROSCOPE

Devices it lists

DeviceProduct codeClassRoleSource
ArthroscopeHRX2Manufactureraccessdata.fda.gov
Laparoscope, Gynecologic (And Accessories)HET2Manufactureraccessdata.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
July 1, 1996K960347SAFETY TROCER WITH SPRINGLOADED OBDURATORHETSubstantially EquivalentSpiess Design, Inc.accessdata.fda.gov
July 25, 1989K894303MEDSCOPE 4MM ARTHROSCOPEHRXSubstantially EquivalentMedscope Corp.accessdata.fda.gov

Compare with other makers

Updated July 1, 1996. 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.