Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 4 companies' records, each linked to the record.
As of Nov 15, 2026, FDA's public records list Teladoc Health and its 4 subsidiaries with 5 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Jun 4, 2020: Livongo Blood Glucose Monitoring System (BG1000).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Teladoc Health and its 4 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 4, 2020 | Livongo Blood Glucose Monitoring System (BG1000)K200277 · NBW | 510(k) clearances |
| Mar 25, 2019 | InTouch Thermal CameraK181716 · LHQ | 510(k) clearances |
| Feb 18, 2016 | The Livongo Health In Touch¿ Blood Glucose Monitoring System (BGMS), is an Over-The-Counter (OTC) system designed for the self- monitoring oClass II · The instructional insert for the In Touch Control Solution for use with the In Touch meter and In Touch strips as a qua | Device recalls |
| Nov 20, 2012 | REMOTE PRESENCE SYSTEM, MODEL RP-VITAK123229 · DRG | 510(k) clearances |
| May 24, 2012 | REMOTE PRESENCE SYSTEMK120895 · DRG | 510(k) clearances |
| Apr 11, 2008 | INTOUCH REMOTE PRESENCE ROBOTIC SYSTEM, MODEL RP-7K073710 · DRG | 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
