FDA applicant

Sriram Enterprises D.B.A. Momentum Group

Orlando, FL1 decision1998–19980 recalls

FDA records 1 decision for Sriram Enterprises D.B.A. Momentum Group (Orlando, FL) in 1998: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). 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, physical medicine panel, where it files most

How often FDA has decided Sriram Enterprises D.B.A. Momentum Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sriram Enterprises D.B.A. Momentum Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sriram Enterprises D.B.A. Momentum Group by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Sriram Enterprises D.B.A. Momentum Group

Which product codes does it file in?

What has FDA decided for it lately?