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 14, 2026, FDA's public records list Sontek Industries with 7 510(k) clearances. The most recent is a 510(k) clearance dated Nov 3, 1983: BODIA BRONCH-SAF DOUBLE SWIVEL.
| Nov 3, 1983 | BODIA BRONCH-SAF DOUBLE SWIVELK833373 · BZA | 510(k) clearances |
| Nov 3, 1983 | BODIA TRACH-SAF DOUBLE SWIVELK833372 · BZA | 510(k) clearances |
| Nov 3, 1983 | BITE-BLOCKK833374 · JAY | 510(k) clearances |
| Nov 3, 1983 | TUBE-TITLEK833361 · JAY | 510(k) clearances |
| Dec 29, 1981 | BODAI SWIVEL YK813324 · BSY | 510(k) clearances |
| Nov 5, 1981 | BODAI PATIENT COMMUNICATORK812720 · ILQ | 510(k) clearances |
| May 27, 1981 | BODAI SUCTION -SAFE 4K811241 · BSY | 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
