Home › Device types › LQZ
Device, Jaw Repositioning
FDA product code LQZ · Class 2 · Dental
199
Registered devices
19
Adverse events
0
Recalls
27
510(k) clearances
Devices with this code
Emerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabSML — SELANE PRODUCTS, INC.Emerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabSlow Wave — Slow Wave, Inc.NAPA Appliance — Great Lakes Dental Technologies, Ltd.Emerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabSML — SELANE PRODUCTS, INC.Emerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabSML — SELANE PRODUCTS, INC.Emerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabEmerald Herbst — Island Dental Lab Inc. DBA Emerald Dental LabKAVA HERBST DUAL LAMINATE — APEX DENTAL SLEEP LAB INCORPORATED
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
