FAICO Dental Implant System and CAD/CAM Abutments

FDA 510(k) Premarket Notification · Submission K211871 · Applicant: Faico Medical, LLC

Public Record 510(k) Submission Decision Date: 2021-11-18 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K211871.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K211871
Applicant / Sponsor
Device Name
FAICO Dental Implant System and CAD/CAM Abutments
Product Code
NHA
Decision Date
2021-11-18
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Dental (DE)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2021-06-17

Related Establishments / Registrations

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