FDA applicant

Intermedics/Infusaid, Inc.

Norwood, MA3 decisions1985–19860 recalls

FDA records 3 decisions for Intermedics/Infusaid, Inc. (Norwood, MA) from 1985 to 1986: 3 510(k) clearances. All are in product code LJT (Port & Catheter, Implanted, Subcutaneous…). 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, general hospital panel, where it files most

How often FDA has decided Intermedics/Infusaid, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intermedics/Infusaid, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Intermedics/Infusaid, 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 “Intermedics/Infusaid”

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

Intermedics, Inc. 211 Intermedics Orthopedics 108 Intermedics Intraocular, Inc. 4

Intermedics/Infusaid, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Intermedics/Infusaid”