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 Medishield, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Sep 27, 1978: SPECTRASCAN.
| Date | Record | Source |
|---|---|---|
| Sep 27, 1978 | SPECTRASCANK781103 · DAT | 510(k) clearances |
| May 3, 1978 | HMD-2000 BATTERY-POWERED MINI-DRILL, THEK780645 · KIJ | 510(k) clearances |
| Apr 28, 1978 | AIR-PWOERED COLDRILLK780646 · EKX | 510(k) clearances |
| Feb 21, 1978 | MONOMER EVACUATION SYSTEMK780202 · JDY | 510(k) clearances |
| Jan 26, 1977 | MICROFENESTRATED HIP REPLACEMENT COMPON.K770161 · JDG | 510(k) clearances |
| Nov 23, 1976 | ANKLE INSTRUMENTS (FREEMAN-SWANSON)K761021 · HSN | 510(k) clearances |
| Nov 23, 1976 | ANKLE (FREEMAN-SWANSON)K761020 · HSN | 510(k) clearances |
| Sep 27, 1976 | SELECTATEC SYSTEMK760668 · CAD | 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
