510(k) Report

FDA applicant

Lsvp Intl., Inc.

Los Altos Hills, CA4 decisions1994–19980 recalls

FDA records 4 decisions for Lsvp Intl., Inc. (Los Altos Hills, CA) from 1994 to 1998: 4 510(k) clearances. Most are in product codes LQR (Dislodger, Stone, Biliary) and EOQ (Bronchoscope (Flexible Or Rigid)). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Lsvp Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lsvp Intl., 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?

  • LQRDislodger, Stone, Biliary1decision
  • EOQBronchoscope (Flexible Or Rigid)1decision
  • KGEForceps, Biopsy, Electric1decision
  • FCLForceps, Biopsy, Non-Electric1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K971204LSVP International Hot Biopsy ForcepsLsvp Intl., Inc. · 19971cites it

What has FDA decided for it lately?

  • K982983LSVP International Biopsy ForcepsLsvp Intl., Inc. · 1998
  • K971204LSVP International Hot Biopsy ForcepsLsvp Intl., Inc. · 1997
  • K945295LSVP International Grasping ForcepsLsvp Intl., Inc. · 1995
  • K944770LSVP International Biopsy ForcepsLsvp Intl., Inc. · 1994

All 4 as Lsvp Intl., Inc. →