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 Sein Electronics with 12 510(k) clearances. The most recent is a 510(k) clearance dated Dec 7, 2005: SEIN BLOOD GLUCOSE AND BLOOD PRESSURE MONITOR SYSTEM, MODEL BGP-100.
| Date | Record | Source |
|---|---|---|
| Dec 7, 2005 | SEIN BLOOD GLUCOSE AND BLOOD PRESSURE MONITOR SYSTEM, MODEL BGP-100K052108 · NBW | 510(k) clearances |
| Aug 24, 2004 | FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR MODEL# SE-311K042138 · DXN | 510(k) clearances |
| Aug 6, 2004 | DIGITAL BLOOD PRESSURE MONITOR, MODELS SE-9000, SE-9200 AND SE-9400K042014 · DXN | 510(k) clearances |
| May 7, 2004 | FULL AUTO ARM DIGITAL BLOOD PRESSURE MONITORK032927 · DXN | 510(k) clearances |
| Aug 8, 2001 | FULL AUTO WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL SE-312K012054 · DXN | 510(k) clearances |
| Dec 15, 2000 | AMBULATORY BLOOD PRESSURE MONITORING SYSTEM, MODEL SE-25M/25PK003711 · DXN | 510(k) clearances |
| Nov 1, 2000 | FULL AUTO BLOOD PRESSURE MONITOR, MODEL SE-7700HK003282 · DXN | 510(k) clearances |
| Feb 11, 2000 | TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR SE-30 TENSK991397 · GZJ | 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
