510(k) Report

FDA applicant

Line One Laboratories & Trading Co.

Los Angeles, CA3 decisions1995–19960 recalls

FDA records 3 decisions for Line One Laboratories & Trading Co. (Los Angeles, CA) from 1995 to 1996: 3 510(k) clearances. All are in product code HIS (Condom). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Line One Laboratories & Trading Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Line One Laboratories & Trading Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Line One Laboratories & Trading Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Line”

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