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 Rudolph Beaver, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 13, 1988: ARTHRO-TRAC(TM).
| Oct 13, 1988 | ARTHRO-TRAC(TM)K883361 · HRX | 510(k) clearances |
| May 3, 1988 | OCU-1K875030 · HMX | 510(k) clearances |
| Aug 1, 1986 | MECHANICAL CYSTITOMEK862709 · HNY | 510(k) clearances |
| Feb 12, 1986 | BEAVER MICRO-GEM GAUGE BLOCKK860305 · HNN | 510(k) clearances |
| Nov 4, 1985 | BEAVER R-K KNIFEK852828 · HNN | 510(k) clearances |
| Aug 6, 1985 | BEAVER MULTIPURPOSE SAPPHIRE KNIFEK853129 · HNN | 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
