FDA applicant

Prism Technologies, Inc.

Washington, DC5 decisions1991–19986 recalls

FDA records 5 decisions for Prism Technologies, Inc. (Washington, DC) from 1991 to 1998: 5 510(k) clearances. Most are in product codes IMD (Pack, Hot Or Cold, Disposable) and HDB (Extractor, Vacuum, Fetal). 6 recalls are 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 Prism Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Prism Technologies, Inc. since 2007.

Recalls per year

1in 2019

2007high 4 (2015) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Prism”

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

Prism Imaging, Inc. 4 Prism Enterprises, Inc. 4 Prism Clinical Imaging, Inc. 2 Prism Therapeutics, LLC 1 Prism Surgical Design Pty, Ltd. 1 Prism Surgical Designs Pty, Ltd. 1

Prism Technologies, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Prism”