FDA 510(k) clearance · back to tracker

Endo Motor (E-LITE MAX, E-LITE PRO, E-LITE INO)

Shenzhen Rogin Medical Co., Ltd. cleared K242514 on 2025-04-24, decision: substantially equivalent

K-number

K242514

Sponsor

Shenzhen Rogin Medical Co., Ltd.

Device

Endo Motor (E-LITE MAX, E-LITE PRO, E-LITE INO)

Class

Class I

Decision

Substantially Equivalent

Decision date

2025-04-24

Product code

EKX

Advisory committee

Dental

Medical specialty

Dental

Regulation number

872.4200

Official FDA record

Open K242514on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Drop K242514 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.