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 14, 2026, FDA's public records list Mist with 8 510(k) clearances. The most recent is a 510(k) clearance dated Sep 26, 1997: MIST MICRO INTERCHANGEABLE SCOPE SYSTEM (TM).
| Sep 26, 1997 | MIST MICRO INTERCHANGEABLE SCOPE SYSTEM (TM)K970937 · GCJ | 510(k) clearances |
| Sep 23, 1997 | MIST PANORAMIC LAPAROSCOPE A RIGID LAPAROSCOPEK971150 · GCJ | 510(k) clearances |
| Jun 23, 1995 | MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES, SURGICAL INSTRUMENTS USED DURING ENDOSCOPIC PROCEDURESK952290 · JOS | 510(k) clearances |
| Jun 23, 1995 | MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZESK952323 · JOS | 510(k) clearances |
| May 12, 1995 | MIST ENDOSCOPIC NEEDLESK951648 · FBK | 510(k) clearances |
| May 3, 1995 | MIST ENDOSCOPIC CANNULASK951481 · GCJ | 510(k) clearances |
| May 3, 1995 | MIST ENDOSCOPIC PROBESK951692 · GCJ | 510(k) clearances |
| May 3, 1995 | MIST TROCARSK951480 · GCJ | 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
