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 15, 2026, FDA's public records list Veran Medical Technologies, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Feb 19, 2021: SPiN Vision Video Bronchoscope 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.
| Feb 19, 2021 | SPiN Vision Video Bronchoscope SystemK202346 · EOQ | 510(k) clearances |
| May 15, 2017 | SPiN Thoracic Navigation SystemK170023 · JAK | 510(k) clearances |
| Dec 21, 2012 | SPIN DRIVE ALWAYS-ON TIP TRACKED STEERABLE CATHETER ALWAYS-ON TIP TRACKED SHEATH ALWAYS-ON TIP TRACKED ASPIRATION NEEDLEK122106 · JAK | 510(k) clearances |
| Jan 27, 2010 | IG 4 IMAGE GUIDED SYSTEMK093995 · JAK | 510(k) clearances |
| Dec 2, 2009 | IG4 ENDOBRONCHIAL, MODEL SYS-0200, NAVIGATION GUIDEWIRE (ACCESSORY TO IG4 ENDOBRONCHIAL), MODEL INS-0300K091934 · JAK | 510(k) clearances |
| Nov 30, 2009 | IG4 IMAGE GUIDED SYSTEM, MODEL: SYS-0200K093146 · JAK | 510(k) clearances |
| May 11, 2006 | IG4 IMAGE GUIDED SYSTEMK060903 · JAK | 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
