FDA applicant

Reimers Systems, Inc.

Springfield, VA5 decisions1995–20110 recalls

FDA records 5 decisions for Reimers Systems, Inc. (Springfield, VA) from 1995 to 2011: 5 510(k) clearances. All are in product code CBF (Chamber, Hyperbaric). Its devices cite 4 predicates, 2 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, anesthesiology panel, where it files most

How often FDA has decided Reimers Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2007high 1 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Reimers Systems, Inc.’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 “Reimers”

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

Reimers and Janssen GmbH 2 Reimers Engineering, Inc. 1

Reimers Systems, Inc.

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 “Reimers”