Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Armstrong Industries, Inc. and its 1 subsidiaries with 9 510(k) clearances. The most recent is a 510(k) clearance dated Sep 25, 2012: STERLING MEDICAL IMPULSE 3 STIMULATOR.
| Sep 25, 2012 | STERLING MEDICAL IMPULSE 3 STIMULATORK121305 · GZJ | 510(k) clearances |
| Sep 10, 1997 | IMPULSE HVGK970847 · IPF | 510(k) clearances |
| Apr 25, 1997 | SIMPLEX TENSK953982 · GZJ | 510(k) clearances |
| Sep 6, 1989 | STERLING TENSK891118 · GZJ | 510(k) clearances |
| Oct 9, 1985 | ELECTROCARDIOGRAPHK852181 · DPS | 510(k) clearances |
| Oct 9, 1985 | SCHILLER MINISCOPE MS-2 EKG SCOPEK852282 · DPS | 510(k) clearances |
| Oct 9, 1985 | SCHILLER EKG COMBI MSG-IM SCOPE & RECORDERK852281 · DPS | 510(k) clearances |
| May 21, 1985 | LARYNGOSCOPEK851705 · CCW | 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
