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 Micromed Development Corp. with 14 510(k) clearances. The most recent is a 510(k) clearance dated May 14, 1996: POLY/PLATINUM WIRE PISTON.
| Date | Record | Source |
|---|---|---|
| May 14, 1996 | POLY/PLATINUM WIRE PISTONK945105 · ETB | 510(k) clearances |
| Jan 20, 1995 | DISPOSABLE JOINT ASPIRATION/INJECTION DIAGNOSTIC KITK945831 · LRO | 510(k) clearances |
| Dec 27, 1994 | NERVE MONITOR ELECTRODES/STIMULATOR PROBESK945242 · ETN | 510(k) clearances |
| Nov 22, 1994 | POLY-WIRE PISTONK945107 · ETB | 510(k) clearances |
| Nov 22, 1994 | MICROMED TOTAL REGULAR AND PARTIAL OFFSETK945106 · ETA | 510(k) clearances |
| Nov 22, 1994 | EDI-BUR MICRODRILL SYSTEMSK945438 · ERL | 510(k) clearances |
| Nov 22, 1994 | POLY PISTONK945108 · ETB | 510(k) clearances |
| Nov 22, 1994 | MICROMED PARTIAL REGULAR AND PARTIAL OFFSETK945104 · ETB | 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
