Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Bio Protech, Inc. with 17 510(k) clearances. The most recent is a 510(k) clearance dated Aug 29, 2019: EvaQMax Smoke Evacuation System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Aug 29, 2019 | EvaQMax Smoke Evacuation SystemK192035 · FYD | 510(k) clearances |
| Jun 3, 2016 | Disposable Concentric Needle electrodes, Disposable Monopolar Needle electrodes, Disposable EP Needle electrodes, Disposable Hypodermic Needle electrodesK152984 · IKT | 510(k) clearances |
| Mar 21, 2016 | Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup ElectrodesK153019 · GXY | 510(k) clearances |
| Jul 16, 2015 | PROPENCIL Smoke PencilK143103 · GEI | 510(k) clearances |
| Nov 17, 2014 | CUTANEOUS ELECTRODESK142099 · GXY | 510(k) clearances |
| Sep 13, 2011 | REUSABLE STIMULATING ELECTRODESK111270 · GXY | 510(k) clearances |
| Nov 24, 2010 | MAX-IF1000K100246 · LIH | 510(k) clearances |
| Nov 30, 2009 | MAXEMS, MODELS 1000 AND 2000K091248 · IPF | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
