Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of OpsensLabelled by claude-sonnet-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 Fiberoptic Sensor Technologies, Inc. with 11 510(k) clearances. The most recent is a 510(k) clearance dated May 11, 1995: FST FIBEROPTIC PRESSURE CONVERTER.
| May 11, 1995 | FST FIBEROPTIC PRESSURE CONVERTERK945753 · FEN | 510(k) clearances |
| Apr 7, 1995 | FST CATH-UD, CATHETERK950908 · FEN | 510(k) clearances |
| Feb 9, 1995 | 4-CHANNEL URODYNAMIC MONITOR WITH URO-FLO OPTIONK945495 · EXY | 510(k) clearances |
| Nov 4, 1993 | FST DUAL, DUAL PRESSURE URODYNAMICS MONITORK930171 · FEN | 510(k) clearances |
| Jul 20, 1993 | FST COUNCIL TIP FOLEY CATHETERK922776 · FEN | 510(k) clearances |
| Jul 20, 1993 | URO-PRO 2000K922476 · FAP | 510(k) clearances |
| Jun 18, 1993 | FST CATH UD-DUAL DUAL PRESSURE CATHETERK926088 · FEN | 510(k) clearances |
| Oct 9, 1991 | FST CATH-UD CATHETER, MODIFICATIONK913113 · FEN | 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
