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 13, 2026, FDA's public records list Infinitech with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 1, 1997: INFINITECH BULLET ENDO ILLUMINATED PICK MANIPULATOR.
| Date | Record | Source |
|---|---|---|
| Oct 1, 1997 | INFINITECH BULLET ENDO ILLUMINATED PICK MANIPULATORK972506 · HJM | 510(k) clearances |
| Aug 1, 1997 | INFINITECH MULTI-SPOT SLIT LAMP LASER ADAPTERK971950 · HQF | 510(k) clearances |
| Oct 19, 1995 | INFINITECH HIGH INTENSITY XENON LIGHT SOURCE SYSTEMK951627 · MPA | 510(k) clearances |
| Mar 1, 1994 | INFINITECH OTOPROBEK931264 · GEX | 510(k) clearances |
| Feb 9, 1994 | END-IRRIGATING ENDOILLUMINATORK931546 · FST | 510(k) clearances |
| Feb 7, 1994 | INFINITECH BREATH EZK935441 · BWN | 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
