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 Kronner Medical with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jul 23, 1990: KRONNER SPHERICAL CUTTERS.
| Jul 23, 1990 | KRONNER SPHERICAL CUTTERSK894228 · HWT | 510(k) clearances |
| Nov 7, 1989 | BLOOD GAS SAFETY SYRINGEK895171 · CBT | 510(k) clearances |
| Sep 12, 1989 | KRONNER SACRAL PIN GUIDEK895172 · LXH | 510(k) clearances |
| Sep 12, 1989 | SKELETAL FIXATION PINK895173 · JDW | 510(k) clearances |
| Jun 3, 1987 | KRONNER COLLES-FOREARM EXTERNAL FIXATIONK871248 · KTT | 510(k) clearances |
| May 22, 1987 | KRONNER UNIVERSAL FRAME EXTERNAL FIXATIONK871247 · KTT | 510(k) clearances |
| May 22, 1987 | KRONNER BI-PLANER TIBIA EXTERNAL FIXATIONK871249 · KTT | 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