FDA applicant

Paramed Div

Knoxville, TN1 decision1992–19920 recalls

FDA records 1 decision for Paramed Div (Knoxville, TN) in 1992: 1 510(k) clearance. All are in product code BXB (Exerciser, Powered). 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 Paramed Div’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paramed Div since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Paramed”

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

Paramed S.R.L. 8 Paramed Technology, Inc. 3 Paramed Services, Inc. 1

Paramed Div

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Paramed”