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 Sterne Equipment Co., Ltd. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 15, 2001: NEURO-TRAIN III (3).
| Jun 15, 2001 | NEURO-TRAIN III (3)K003433 · IPF | 510(k) clearances |
| Jul 28, 1998 | MYO-TRAIN V (5)K980158 · IPF | 510(k) clearances |
| Oct 8, 1997 | ACU-RAY HF SERIES PORTABLE X-RAY UNITK972204 · IZL | 510(k) clearances |
| Mar 17, 1997 | NEURO-TRAIN II (2)K970155 · IPF | 510(k) clearances |
| Nov 3, 1993 | ACU-RAYK931279 · IZL | 510(k) clearances |
| Jul 14, 1989 | NEUROTRAINK883896 · LIH | 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
