510(k) Report

FDA applicant

Innovative Technologies (Us), Inc.

Golden,, CO3 decisions1998–19980 recalls

FDA records 3 decisions for Innovative Technologies (Us), Inc. (Golden,, CO) in 1998: 3 510(k) clearances. Most are in product codes KMF (Bandage, Liquid) and 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

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Innovative Technologies (Us), Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Innovative Technologies (Us), Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Innovative Technologies (Us), 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?

  • KMFBandage, Liquid1decision
  • MGQDressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic1decision
  • MGPDressing, Wound And Burn, Occlusive1decision

What has FDA decided for it lately?

  • K982804Spyrogel Hydrogel Wound and Burn DressingInnovative Technologies (Us), Inc. · 1998
  • K980673Spyrosorb Foam Island Wound DressingInnovative Technologies (Us), Inc. · 1998
  • K974520Spyroflex Foam Island Wound Dressing, Spyroflex Foam Island Wound Dressing, Tinted, SpyrofoamInnovative Technologies (Us), Inc. · 1998

All 3 as Innovative Technologies (Us), Inc. →