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 15, 2026, FDA's public records list Pedicraft with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 20, 1993: PEDICRAGT BASSINET.
| Apr 20, 1993 | PEDICRAGT BASSINETK925949 · FMS | 510(k) clearances |
| Apr 20, 1993 | HEAD & FOOT END DROP PEDI-CRIBK925817 · FMS | 510(k) clearances |
| Mar 13, 1991 | PEDICRAFT INFANT REFLUX WEDGEK905629 · FRP | 510(k) clearances |
| Mar 13, 1991 | INFANT REFLUX SLINGK905630 · FRP | 510(k) clearances |
| Jun 23, 1982 | PEDICRAFT BED, MODEL B2944K821773 · FMS | 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
