FDA applicant

Boston Foundation For Sight

Needham, MA1 decision2016–20160 recalls

FDA records 1 decision for Boston Foundation For Sight (Needham, MA) in 2016: 1 510(k) clearance. All are in product code HQD (Lens, Contact (Other Material) - Daily). Its devices cite 3 predicates, 0 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, ophthalmic panel, where it files most

How often FDA has decided Boston Foundation For Sight’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Boston Foundation For Sight by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Boston Foundation For Sight’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Boston”

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

Boston Scientific Corp 809 Boston Scientific Scimed, Inc. 40 Boston Medical Products, Inc. 33 Boston Scientific, Target 19 Boston Surgical Products, Inc. 17 Boston Biomedica, Inc. 12 Boston Scientific Neuromodulation 11 Boston Pacific Medical, Inc. 11 Boston Medical Corp. 8 Boston Aesthetics, Inc. 6 The Boston Medical Group 5 Boston Scientific/Medi-Tech 5

Boston Foundation For Sight

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 “Boston”