FDA applicant

Medapps Inc., Dba Alere Connect

Scottsdale, AZ2 decisions2013–20130 recalls

FDA records 2 decisions for Medapps Inc., Dba Alere Connect (Scottsdale, AZ) in 2013: 2 510(k) clearances. All are in product code DRG (Transmitters And Receivers, Physiological…). Its devices cite 6 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 Medapps Inc., Dba Alere Connect’s devices, and how often a recall has named them.

FDA decisions per year

2in 2013

2013high 2 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Medapps Inc., Dba Alere Connect by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medapps Inc., Dba Alere Connect’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Medapps”

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

Medapps, Inc. 3

Medapps Inc., Dba Alere Connect

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Medapps”