FDA applicant

Mednet Locator, Inc.

Memphis, TN9 decisions1997–20000 recalls

FDA records 9 decisions for Mednet Locator, Inc. (Memphis, TN) from 1997 to 2000: 9 510(k) clearances. Most are in product codes ETD (Tube, Tympanostomy) and ETA (Replacement, Ossicular Prosthesis, Total). 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, ear, nose and throat panel, where it files most

How often FDA has decided Mednet Locator, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mednet Locator, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mednet Locator, Inc.’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 “Mednet”

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

Mednet, Inc. 12 Mednet Services, Inc. 2

Mednet Locator, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mednet”