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 Myo/Kinetic Systems, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jul 14, 1995: TE-800 PELVIC FLOOR EXERCISER.
| Jul 14, 1995 | TE-800 PELVIC FLOOR EXERCISERK945937 · HIR | 510(k) clearances |
| Apr 12, 1995 | TS-700P CONTROL XP ELECTRICAL STIMULATORK945292 · KPI | 510(k) clearances |
| Mar 8, 1995 | URO-GRAM CYSTOMRTROGRAM WITH UROFLOWMETRYK944972 · EXY | 510(k) clearances |
| Apr 18, 1994 | UROGRAM CYSTOMETROGRAMK936041 · FEN | 510(k) clearances |
| Jan 31, 1994 | NEUROMUSCULAR STIMULATORK932611 · GZJ | 510(k) clearances |
| Oct 1, 1993 | THERAPEUTIC STIMULATOR 300(TS-300) & 300P(TS-300P)K932764 · IPF | 510(k) clearances |
| Aug 11, 1993 | THERAPEUTIC STIM 200 (TS-200)/200P (TS-200P)K932399 · IPF | 510(k) clearances |
| Apr 28, 1992 | THERAPEUTIC STIMULATOR 2100 (TS-2100)K914904 · IPF | 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
