KeYi Total Hip System— 510(k) K191826

Name: FDA 510(k) clearance K191826
Creator: U.S. Food and Drug Administration
Published: 2020-05-14

Substantially Equivalent

Beijing Keyi Medical Device Technology Co., Ltd.

FDA 510(k) clearance K191826 for KeYi Total Hip System, Substantially Equivalent on 2020-05-14. Applicant: Beijing Keyi Medical Device Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Beijing Keyi Medical Device Technology Co., Ltd.
Product code: Code LPH
Device class: Class 2
Regulation: 21 CFR 888.3358
Advisory panel: Orthopedic
Date received: 2019-07-08
Decision date: 2020-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beijing, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code LPH

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K253630 — Mpact 3D Metal Foam2026-08-28
K254043 — TRIVANCE Hip Stem2026-08-04
K261624 — Omnifit® 20° Series I Insert +11 more2026-07-10
K243192 — iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating2026-06-05
K251270 — Taperloc® Complete Hip Stem2026-05-19

More clearances from Beijing Keyi Medical Device Technology Co., Ltd.

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K230120 — KeYi Total Knee System2024-04-19
K190567 — KeYi Spinal Fixation System2019-05-08
K162380 — Locking Plate System2017-05-02

Adverse events under product code LPH

product code LPH

Death: 73
Injury: 31,640
Malfunction: 3,358
Other: 2
Total: 35,073

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.