FDA applicant

Inter-Med / Vista Dental

Racine, WI1 decision2021–20210 recalls

FDA records 1 decision for Inter-Med / Vista Dental (Racine, WI) in 2021: 1 510(k) clearance. All are in product code KJJ (Cleanser, Root Canal). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Inter-Med / Vista Dental’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Inter-Med / Vista Dental by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Inter-Med / Vista Dental’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Inter-Med”

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-Os Technologies 2 Inter Continental Health Care 2 Inter-Asia Co., Inc. 1 Inter-Pal GmbH 1 Inter-Continental Industries Sdn Bhd 1

Inter-Med / Vista Dental

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Inter-Med”