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 Biomedical Life Systems with 37 510(k) clearances. The most recent is a 510(k) clearance dated Jul 8, 2018: BMLS16-1.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 8, 2018 | BMLS16-1K172971 · NUH | 510(k) clearances |
| Jul 29, 2011 | PAIN BUDDYK102051 · NUH | 510(k) clearances |
| Jul 26, 2006 | ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS06-1K061476 · GZJ | 510(k) clearances |
| Mar 14, 2005 | MODEL BMLS03-7K042711 · GZJ | 510(k) clearances |
| Nov 23, 2004 | COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL STIMULATOR, MODEL BMLS04-1K041388 · GZJ | 510(k) clearances |
| Jul 7, 2004 | INTERFERENTIAL STIMULATOR, MODEL BMLS02-6K040007 · LIH | 510(k) clearances |
| Jun 30, 2004 | BMLS03-3K033174 · IPF | 510(k) clearances |
| Apr 29, 2004 | INTERFERENTIAL STIMULATOR, MODEL BMLS03-6K040824 · LIH | 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
