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 15, 2026, FDA's public records list H&P Industries, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 22, 1990: TRIA-SONIC ULTRA SOUND TRANSMISSION GEL.
| Jun 22, 1990 | TRIA-SONIC ULTRA SOUND TRANSMISSION GELK901217 · JOT | 510(k) clearances |
| Apr 1, 1987 | LUBRICATING JELLYK871169 · KMJ | 510(k) clearances |
| Apr 9, 1986 | GAMMA RADIATION STERILIZED ALCOHOL PREP PADSK860961 · LKB | 510(k) clearances |
| Apr 6, 1983 | PROVIDONE-IODINE PREP-PADS & TOWELETTESK830394 · GEC | 510(k) clearances |
| Apr 6, 1983 | PROVIDONE-IODINE SWABSTICKSK830393 · GEC | 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
