Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Thrombolex, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 3, 2023: BASHIR™ .035 Endovascular Catheter, BASHIR™ S-B .035 Endovascular Catheter.
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 |
|---|---|---|
| Jul 3, 2023 | BASHIR™ .035 Endovascular Catheter, BASHIR™ S-B .035 Endovascular CatheterK231653 · QEY | 510(k) clearances |
| Apr 20, 2023 | BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101K222095 · QEY | 510(k) clearances |
| Jun 10, 2021 | BASHIR Endovascular Catheter (Ref. 7201), BASHIR Plus 10 Endovascular Catheter (Ref. 7210), BASHIR Plus 20 Endovascular Catheter (Ref. 7220), BASHIR Plus 30 Endovascular Catheter (Ref. 7230), BASHIR Plus 40 Endovascular Catheter (Ref. 7240)K211061 · QEY | 510(k) clearances |
| Dec 17, 2019 | Bashir Plus Endovascular CatheterK193071 · QEY | 510(k) clearances |
| Oct 18, 2019 | Bashir S-B Endovascular Catheter, Ref. No. 7101K192598 · QEY | 510(k) clearances |
| Feb 25, 2019 | Bashir Endovascular Catheter Model 7201, Bashir N-X Endovascular Catheter, Mode 7200K183290 · QEY | 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
