FDA applicant

Telos Medical Corp.

Keene, CA7 decisions1988–19920 recalls

FDA records 7 decisions for Telos Medical Corp. (Keene, CA) from 1988 to 1992: 7 510(k) clearances. Most are in product codes DQO (Catheter, Intravascular, Diagnostic) and KXO (Monitor, Pressure, Intrauterine). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Telos Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Telos Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Telos Medical Corp.’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 “Telos”

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

The Telos Co. 2 Telos Medical Equipment 1

Telos Medical Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Telos”