FDA applicant

Weck Surgical Systems

Hauppauge, NY1 decision1987–19870 recalls

FDA records 1 decision for Weck Surgical Systems (Hauppauge, NY) in 1987: 1 510(k) clearance. All are in product code LKW (Laser, Neurosurgical). 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 Weck Surgical Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Weck Surgical Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Weck Surgical Systems’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 “Weck”

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

Weck Closure Systems 6 Weck Endoscopy 4 Weck 2

Weck Surgical Systems

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Weck”