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Contra-Angle (1059 +15 more)

FDA 510(k)

Class I (US FDA 510(k))

510(k) K022505

by Nouvag AG

Identifiers

510(k) Number
K022505 FDA 510(k)
FDA Product Code
EGS FDA 510(k)
Models / Variants
1059 FDA 510(k)
5050 FDA 510(k)
5051 FDA 510(k)
5055 FDA 510(k)
5056 FDA 510(k)
5057 FDA 510(k)
5059 FDA 510(k)
5060 FDA 510(k)
5061 FDA 510(k)
5062 FDA 510(k)
5063 FDA 510(k)
5064 FDA 510(k)
5065 FDA 510(k)
5066 FDA 510(k)
5067 FDA 510(k)
5068 FDA 510(k)

Classification

Device Class
Class I FDA 510(k)
Legislation / Framework
21 CFR Part 872.4200 FDA 510(k)
Regulation Number
872.4200 FDA 510(k)
Advisory Committee
Dental FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Contra-Angle (1059 +15 more) by Nouvag AG — Class I — FDA_510K — listed in FDA 510(k) — 16 models — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Nouvag AG

Sources (1)

  • FDA 510(k) K022505 24 fields · synced Jun 18, 2026