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Ultranovar, Dental U.V. Curing Lamp

by Demetron Research Corp. 510(k)

Active United States

510(k) K780518

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK780518 Date28 Apr 1978ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
EBZ
Device Class
Class II
Regulation
21 CFR Part 872.6070
Advisory Committee
Dental
FDA Decision
SESE Substantially Equivalent

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