510(k) Report

FDA applicant

Phytatek Laboratories, Inc.

Washington, DC1 decision1998–19980 recalls

FDA records 1 decision for Phytatek Laboratories, Inc. (Washington, DC) in 1998: 1 510(k) clearance. All are in product code MGQ (Dressing, Wound And Burn, Hydrogel W/Drug…). 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 Phytatek Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Phytatek Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Phytatek Laboratories, 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?

  • MGQDressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic1decision

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.

  • K980132Phytacare Alginate Hydrogel Wound DressingPhytatek Laboratories, Inc. · 19981cites it

What has FDA decided for it lately?

  • K980132Phytacare Alginate Hydrogel Wound DressingPhytatek Laboratories, Inc. · 1998

The one decision as Phytatek Laboratories, Inc. →