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 KMN Products, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Dec 9, 1982: KM-KAL L3.
| Dec 9, 1982 | KM-KAL L3K823044 · JIX | 510(k) clearances |
| Nov 16, 1982 | KM - KAL 5K823021 · JIT | 510(k) clearances |
| Nov 16, 1982 | KM-KAL 3K823019 · JIT | 510(k) clearances |
| Nov 16, 1982 | KM - KAL 2K823025 · JIT | 510(k) clearances |
| Nov 16, 1982 | KM-KAL L6K823023 · JIT | 510(k) clearances |
| Nov 16, 1982 | KM-KAL 6K823022 · JIT | 510(k) clearances |
| Nov 16, 1982 | KM-KAL 4K823020 · JIT | 510(k) clearances |
| Nov 16, 1982 | KM - KAL 1K823024 · JIT | 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
