Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 5 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Scottcare Corporation with 7 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Jun 4, 2025: TeleRehab Aermos Cardiopulmonary Rehabilitation.
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.
| Date | Record | Source |
|---|---|---|
| Jun 4, 2025 | TeleRehab Aermos Cardiopulmonary RehabilitationK250259 · DRG | 510(k) clearances |
| Feb 25, 2016 | TeleSentry Battery, 3.7 Li-Ion Polymer Battery, CAUTION Do not expose to high temperature. Do not disassemble. Dispose of properly. Use specClass II · The firm received a complaint of the battery exploding while recharging. | Device recalls |
| Dec 12, 2014 | TELESENSEK142180 · DSI | 510(k) clearances |
| Feb 26, 2010 | TELESENTRY, MODEL TS01K092947 · DSI | 510(k) clearances |
| Aug 13, 2009 | CHROMA, MODEL: RZ153CK083382 · MWJ | 510(k) clearances |
| May 29, 2008 | GENESIS ECPK081359 · DRN | 510(k) clearances |
| Apr 13, 2005 | TELEREHAD 2004K050778 · DRG | 510(k) clearances |
| Mar 6, 1990 | TELEREHAB SYSTEM FOR CARDIAC REHABILITATIONK895719 · DXH | 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
