510(k) Report

FDA applicant

Tava Surgical Instruments

Van Nuys, CA7 decisions1986–19941 recall

FDA records 7 decisions for Tava Surgical Instruments (Van Nuys, CA) from 1986 to 1994: 7 510(k) clearances. Most are in product codes HSZ (Instrument, Surgical, Orthopedic, Pneumatic…) and GFA (Blade, Saw, General & Plastic Surgery, Surgical). 1 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 Tava Surgical Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tava Surgical Instruments since 2007.

Recalls per year

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Tava Surgical Instruments’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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