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 Ness Neuromuscular Electrical Stimulation Systems and its 1 subsidiaries with 8 510(k) clearances. The most recent is a 510(k) clearance dated Sep 15, 2011: NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT.
| Sep 15, 2011 | NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KITK111767 · GZI | 510(k) clearances |
| Feb 28, 2008 | MODIFICATION TO:NESS L300K080219 · GZI | 510(k) clearances |
| Jul 7, 2006 | NESS L300K053468 · GZI | 510(k) clearances |
| Aug 8, 2003 | HANDMASTERK031900 · GZI | 510(k) clearances |
| Feb 5, 2003 | NESS CHILDREN SYSTEMK024279 · IPG | 510(k) clearances |
| Sep 11, 2002 | NESS SYSTEMK022776 · IPF | 510(k) clearances |
| Nov 14, 2001 | MODIFICATION TO HANDMASTERK012823 · GZI | 510(k) clearances |
| Sep 30, 1998 | HANDMASTER NMS1K982482 · 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
