FDA applicant
Medical Electronic Devices, Inc.
FDA records 7 decisions for Medical Electronic Devices, Inc. (Torrance, CA) from 1976 to 2005: 7 510(k) clearances. Most are in product codes NFB (Conserver, Oxygen) and DPW (Flowmeter, Blood, Cardiovascular). Its devices cite 11 predicates, 3 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
How often FDA has decided Medical Electronic Devices, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Medical Electronic Devices, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medical Electronic Devices, 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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