FDA applicant

Telstar Electronics, Inc.

Longwood, FL11 decisions1987–19890 recalls

FDA records 11 decisions for Telstar Electronics, Inc. (Longwood, FL) from 1987 to 1989: 11 510(k) clearances. Most are in product codes ESD (Hearing Aid, Air-Conduction, Prescription) and LRS (I.V. Start Kit). 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 Telstar Electronics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Telstar Electronics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Telstar Electronics, Inc.’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 “Telstar”

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

Telstar Innovations, Inc. 1

Telstar Electronics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Telstar”