FDA applicant

Restorative Health Svs, Inc.

Washington, DC1 decision2001–20010 recalls

FDA records 1 decision for Restorative Health Svs, Inc. (Washington, DC) in 2001: 1 510(k) clearance. All are in product code MVA (Orthosis, Cranial). Its devices cite 1 predicate, 0 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Restorative Health Svs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Restorative Health Svs, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Restorative Health Svs, Inc.’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 “Restorative”

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

Restorative Therapies, Inc. 10

Restorative Health Svs, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Restorative”