FDA applicant

Inter-Os Technologies

Lone Tree, CO2 decisions2000–20030 recalls

FDA records 2 decisions for Inter-Os Technologies (Lone Tree, CO) from 2000 to 2003: 2 510(k) clearances. Most are in product codes KTT (Appliance, Fixation, Nail/Blade/Plate…) and MQN (External Mandibular Fixator And/Or Distractor). Its devices cite 8 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Inter-Os Technologies, LLC”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Inter-Os Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inter-Os Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Inter-Os Technologies by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Inter-Os Technologies’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 “Inter-Os”

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

Inter-Med, Inc. 12 Inter-Med/Vista Dental Products 6 Inter Medical Medizintechnik GmbH 3 Inter Med Industries, Inc. 3 Inter Science Institute 3 Inter Continental Health Care 2 Inter-Asia Co., Inc. 1 Inter-Pal GmbH 1 Inter-Med / Vista Dental 1 Inter-Continental Industries Sdn Bhd 1

Inter-Os Technologies

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Inter-Os”