MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER— 510(k) K882063

Name: FDA 510(k) clearance K882063
Creator: U.S. Food and Drug Administration
Published: 1988-06-13

Substantially Equivalent

Zest Anchors, Inc.

FDA 510(k) clearance K882063 for MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER, Substantially Equivalent on 1988-06-13. Applicant: Zest Anchors, Inc.. Device class: 1.

Clearance details

Applicant: Zest Anchors, Inc.
Product code: Code EGG
Device class: Class 1
Regulation: 21 CFR 872.3165
Advisory panel: Dental
Date received: 1988-05-16
Decision date: 1988-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EGG

view all

K990979 — STECO-TITANMAGNETICS1999-09-03
K950259 — COUPLING DEVICE FOR DENTAL PROSTHESIS1996-12-06
K925700 — ZEST ANCHOR ADVANCED GENERATION1994-04-07
K915299 — COGAN CORP KITS OF DENTAL HAND INSTRUMENTS1992-01-31
K912435 — DENTAL CONNECTOR PRECISION ATTACHMENT1991-08-28

More clearances from Zest Anchors, Inc.

view all

K150295 — LOCATOR RTx2015-07-24
K083324 — LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM2009-02-25
K072878 — MODIFICATION TO: LOCATOR IMPLANT ANCHOR2007-12-03
K042466 — X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE2004-11-24
K033699 — LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 085862004-04-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.