510(k) Report

FDA applicant

Circuit Tree

Temple City, CA3 decisions1995–19980 recalls

FDA records 3 decisions for Circuit Tree (Temple City, CA) from 1995 to 1998: 3 510(k) clearances. All are in product code HQC (Unit, Phacofragmentation). 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, ophthalmic panel, where it files most

How often FDA has decided Circuit Tree’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Circuit Tree since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HQCUnit, Phacofragmentation3decisions

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K981989The Wave Digital Phaco SystemCircuit Tree · 19981cites it
  • K954242Circuit Tree PhacoemulsifierCircuit Tree · 19951cites it

What has FDA decided for it lately?

  • K981989The Wave Digital Phaco SystemCircuit Tree · 1998
  • K954237Circuit Tree Phaco HandpieceCircuit Tree · 1995
  • K954242Circuit Tree PhacoemulsifierCircuit Tree · 1995

All 3 as Circuit Tree →

Other applicant names beginning “Circuit”

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

Circuit Tree Medical, Inc. 2