Zest Anchors, Inc.
FDA 510(k) medical device clearances.
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.