Zest Anchors, Inc.
Zest Anchors, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 2015.
Top product codes for Zest Anchors, Inc.
Recent clearances by Zest Anchors, Inc.
- K150295 — LOCATOR RTx
- K083324 — LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM
- K072878 — MODIFICATION TO: LOCATOR IMPLANT ANCHOR
- K042466 — X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE
- K033699 — LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CAST-TO FEMALE, MODELS 08587, 08588, 08586
- K994257 — LOCATOR IMPLANT ANCHOR
- K925849 — ZEST IMPLANT ANCHOR
- K934668 — ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL)
- K925700 — ZEST ANCHOR ADVANCED GENERATION
- K882063 — MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER
- K861561 — ZEST MARK II (STANDARD & MINI)
- K840244 — BIOCERAM ZEST PLANT
- K801524 — ZEST PLANT
- K801525 — ZEST ENDODONTIC STABILIZER
Data sourced from openFDA. This site is unofficial and independent of the FDA.