510(k) Report

FDA applicant

Encore Technology, Inc.

Santa Clara, CA1 decision1989–19890 recalls

FDA records 1 decision for Encore Technology, Inc. (Santa Clara, CA) in 1989: 1 510(k) clearance. All are in product code LYY (Latex Patient Examination Glove). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Encore Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Encore Technology, Inc. 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?

  • LYYLatex Patient Examination Glove1decision

What has FDA decided for it lately?

  • K891425Patient Examination Gloves (Latex)Encore Technology, Inc. · 1989

The one decision as Encore Technology, Inc. →

Other applicant names beginning “Encore”

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

Encore Orthopedics, Inc. 85Encore Medical L.P. 85Encore Guards 2Encore Products, Inc. 2Encore Medical, L.P Dba Enovis 2Encore, Inc. 1Encore Medical, L.P. Dba Djo Surgical 1Encore Medical, L.P. (Dba Enovis) 1