FDA 510(k) clearance · back to tracker
Dental Implant Unit
Guilin Aesthedent Medical Instruments Co., Ltd. cleared K242646 on 2025-04-11, decision: substantially equivalent
K-number
K242646
Sponsor
Guilin Aesthedent Medical Instruments Co., Ltd.
Device
Dental Implant Unit
Class
Class I
Decision
Substantially Equivalent
Decision date
2025-04-11
Product code
EBW
Advisory committee
Dental
Medical specialty
Dental
Regulation number
872.4200
Official FDA record
Open K242646on 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.
Use this as a predicate
Drop K242646 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.
Try the sandboxSource
Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.