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FDA device clearances in Oklahoma

Every FDA 510(k) decision for applicants based in Oklahoma in the last 12 months, with the device, the product area and FDA's own record.

Decisions6
Applicants6

6 premarket notifications (510(k)s) from applicants based in Oklahoma were decided by FDA in the last 12 months, newest first. Each row links to FDA's own record.

DecidedApplicantDeviceAreaWhereRecord
2026-09-23Special Situations, LLCEverslide NUCObstetrics/GynecologyTulsa, OklahomaK260117
2026-07-02BPEndo, LLCInsufflation Retention Device (IRD) (11173-325-101) FDFGastroenterology, UrologyNorman, OklahomaK261587
2026-05-06Biozen, LLCBP1000 Ultra-Compact Fingertip Blood Pressure Monitor (BP1000) DXNCardiovascularOklahoma City, OklahomaK253152
2026-02-23Box Spine, LLCDuet™ Spinal Fixation System NKBOrthopedicTulsa, OklahomaK253169
2026-01-22Perin Health Devices, LLCPerin Health System (PHD80060-2) DRGCardiovascularOklahoma City, OklahomaK252984
2025-12-18Park Dental Research Corp.Park Dental Nylon MAD LRKDentalArdmore, OklahomaK252976

Where this comes from

Before most medical devices can be sold in the United States, the maker submits a premarket notification, a 510(k), and FDA decides whether the device is substantially equivalent to one already on the market. Every row here is one of those decisions, linked to FDA's own record of it. The product area is the medical specialty FDA files the device under; the location is the applicant's, as the submission gives it.

A clearance means the agency found the device substantially equivalent; it is not an endorsement. Where an applicant also files with the SEC under the same name in the same state, it links to that company's page.

All device clearances

Cite this page

Permanent URL: https://mentionfox.com/fda/510k/state/ok
Last updated 2026-10-18
FDA device clearances in Oklahoma: 6 510(k) decisions in the last 12 months. MentionFox, 2026-10-18. https://mentionfox.com/fda/510k/state/ok