DeviceClearance

Rodo Abutment System— 510(k) K193274

Substantially Equivalent

Rodo Medical, Inc.

FDA 510(k) clearance K193274 for Rodo Abutment System, Substantially Equivalent on 2020-02-27. Applicant: Rodo Medical, Inc.. Device class: 2.

Clearance details

Applicant
Rodo Medical, Inc.
Product code
Code NHA
Device class
Class 2
Regulation
21 CFR 872.3630
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
San Jose, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code NHA

product code NHA
Injury
1,270
Malfunction
2,860
Total
4,130

Source: openFDA MAUDE database, through . 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.