510(k) Report

FDA applicant

Encompass Group, LLC

Mcdonough, GA4 decisions1976–20200 recalls

FDA records 4 decisions for Encompass Group, LLC (Mcdonough, GA) from 1976 to 2020: 4 510(k) clearances. Most are in product codes FYA (Gown, Surgical) and FMQ (Restraint, Protective). 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, general and plastic surgery panel, where it files most

How often FDA has decided Encompass Group, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2020: 1
2007high 1 (2020) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Encompass Group, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Encompass Group, LLC’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 “Encompass”

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