FDA applicant

Sacks Model Makers

Ringwood, NJ1 decision1989–19890 recalls

FDA records 1 decision for Sacks Model Makers (Ringwood, NJ) in 1989: 1 510(k) clearance. All are in product code MSI (Solution, Cleaning / Lubricating, Artificial Eye). No recall is linked to its devices.

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

How often FDA has decided Sacks Model Makers’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sacks Model Makers since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sacks Model Makers’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 “Sacks”

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

Sacks Farms Biological Products 3 Sacks Holdings, Inc. 1

Sacks Model Makers

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sacks”