FDA applicant

Multi-Med, Inc.

West Swanzey, NH8 decisions1989–201275 recalls

FDA records 8 decisions for Multi-Med, Inc. (West Swanzey, NH) from 1989 to 2012: 8 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FMI (Needle, Hypodermic, Single Lumen). Its devices cite 1 predicate, 0 of them its own earlier devices. 75 recalls are linked to its devices.

FDA’s records also spell it “Multi Med”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Multi-Med, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

75in 2010

2007high 75 (2010) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Multi-Med, 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 “Multi-Med”

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

Multi Radiance Medical 3 Multi Biosensors, Inc. 2 Multi M Intl., Inc. 2 Multi Trading Corp. of America, Inc. 1 Multi-Com Sdn Bhd 1 Multi-Dimensional Imaging, Inc. 1 Multi-Channel Epilator 1 Multi-Spectrum Consulting, Inc. 1 Multi-Wash Medical, Ltd. 1 Multi Media Dental Systems, Inc. 1

Multi-Med, 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?

What has been recalled?

Other applicant names beginning “Multi-Med”