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 Biomedical Devices, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Dec 26, 1995: THE REEL THING (MODIFICATION).
| Date | Record | Source |
|---|---|---|
| Dec 26, 1995 | THE REEL THING (MODIFICATION)K955439 · GBX | 510(k) clearances |
| Jun 28, 1994 | BIO-PREP CEMENT RESTRICTORK931847 · LZN | 510(k) clearances |
| Jan 21, 1994 | BIO-PREPK931846 · LXH | 510(k) clearances |
| Oct 7, 1993 | BMD AIR/OXYGEN BLENDERK925982 · BZR | 510(k) clearances |
| Oct 19, 1990 | STERI-SHIELDK903533 · FXY | 510(k) clearances |
| Aug 17, 1990 | STERI-SHIELDK902677 · FXY | 510(k) clearances |
| Mar 31, 1983 | PUMP PALL AMBULATORY INSULIN INFUSIONK830605 · FRN | 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
