510(k) Report

FDA applicant

Labtician Products, Inc.

Sarasota, FL1 decision1988–19880 recalls

FDA records 1 decision for Labtician Products, Inc. (Sarasota, FL) in 1988: 1 510(k) clearance. All are in product code HQJ (Implant, Absorbable, (Scleral Buckling Methods)). 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 Labtician Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Labtician Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HQJImplant, Absorbable, (Scleral Buckling Methods)1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K875014Labtician Retinal ImplantsLabtician Products, Inc. · 19881cites it

What has FDA decided for it lately?

  • K875014Labtician Retinal ImplantsLabtician Products, Inc. · 1988

The one decision as Labtician Products, Inc. →

Other applicant names beginning “Labtician”

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

Labtician Ophthalmics, Inc. 4