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Unicide

by North Pacific Dental, Inc.

510(k) K830106

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 11 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 11 Oct 2026. What this means

Regulatory status

as of registry sync 11 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK830106 Date7 Mar 1983ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 11 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
LFE
Device Class
Class II
Regulation
21 CFR Part 880.6885
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Other devices from North Pacific Dental, Inc.

  • Gutta Percha Points

    Class I

  • Vitathyl

    Class II

  • Septopack

    Class II

  • Paper Points

    Class I

  • Septocal

    Not classified

  • Sulcarings

    Class I

See all devices from North Pacific Dental, Inc. →