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 Avid N.I.T. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jul 16, 2002: AVID-NIT NERVE STIMULATION NEEDLES.
| Date | Record | Source |
|---|---|---|
| Jul 16, 2002 | AVID-NIT NERVE STIMULATION NEEDLESK014246 · CAZ | 510(k) clearances |
| Dec 3, 2001 | AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ EPIDURAL NEEDLE, MODEL RM2035LK013231 · BSP | 510(k) clearances |
| Nov 6, 1998 | N,I.T., INC. AUTOMATIC CUTTING BIOPSY NEEDLEK983218 · FCG | 510(k) clearances |
| May 20, 1998 | ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCERK972595 · BSP | 510(k) clearances |
| Feb 17, 1998 | REGANES RADIONUCLIDE SEED MAGAZINEK972554 · IWJ | 510(k) clearances |
| Jan 27, 1998 | N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000K973037 · IWJ | 510(k) clearances |
| Dec 23, 1997 | N.I.T., INC. NEEDLE GUIDING TEMPLATEK973638 · IWJ | 510(k) clearances |
| Aug 1, 1997 | REGANES SPINAL NEEDLE (VARIOUS)K971645 · MIA | 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
