FDA applicant

Accu-Speed, Incorporated

Groton, MA1 decision2003–20030 recalls

FDA records 1 decision for Accu-Speed, Incorporated (Groton, MA) in 2003: 1 510(k) clearance. All are in product code KGS (Retention Device, Suture). 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 and plastic surgery panel, where it files most

How often FDA has decided Accu-Speed, Incorporated’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Accu-Speed, Incorporated since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Accu-Speed”

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

Accu-Line 4 Accu-Stat Diagnostics, Inc. 3 Accu Science Corp. 2 Accu-Med Corp. 1 Accu-Path 1

Accu-Speed, Incorporated

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Accu-Speed”