510(k) Report

FDA applicant

Intouch Health, Inc.

Goleta, CA2 decisions2012–20120 recalls

FDA records 2 decisions for Intouch Health, Inc. (Goleta, CA) in 2012: 2 510(k) clearances. All are in product code DRG (Transmitters And Receivers, Physiological…). Its devices cite 2 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Intouch Health, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2012

2012: 2
2012high 2 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Intouch Health, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DRGTransmitters And Receivers, Physiological Signal, Radiofrequency2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K120895Remote Presence SystemIntouch Health, Inc. · 20121cites it

What has FDA decided for it lately?

  • K123229Remote Presence System, Model RP-VitaIntouch Health, Inc. · 2012
  • K120895Remote Presence SystemIntouch Health, Inc. · 2012

All 2 as Intouch Health, Inc. →

Other applicant names beginning “Intouch”

FDA records each applicant name separately; these may or may not be the same firm.

Intouch Technologies, Inc., D.B.A. Intouch Health 1Intouch Technologies 1