510(k) Report

FDA applicant

Energy Life Systems Corp.

Costa Mesa, CA5 decisions1994–19950 recalls

FDA records 5 decisions for Energy Life Systems Corp. (Costa Mesa, CA) from 1994 to 1995: 5 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). 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, general and plastic surgery panel, where it files most

How often FDA has decided Energy Life Systems Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Energy Life Systems Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Energy Life Systems Corp.’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 “Energy”

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