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Data / Medical devices / United States / Island Dental Lab Dba Emerald Dental Lab

Island Dental Lab Dba Emerald Dental Lab: FDA-registered device maker in Valley Stream, NY, United States, 1 510(k) clearance

Island Dental Lab Dba Emerald Dental Lab is registered with the FDA (registration 3027346720) in Valley Stream, NY, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 10, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3027346720
Address
76 S. Central Ave, # 1D, Valley Stream, NY, United States, 11580
Owner or operator
Island Dental Lab dba Emerald Dental Lab (10088017)
Roles
Manufacturer
First device listed
May 15, 2023
Registered through
2026
Brand names listed
Emerald Herbst

Devices it lists

DeviceProduct codeClassRoleSource
Device, Anti-SnoringLRK2Manufactureraccessdata.fda.gov
Device, Jaw RepositioningLQZ2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 10, 2023K223624Emerald HerbstLRKSubstantially EquivalentIsland Dental Lab, Inc Dba Emerald Dentalaccessdata.fda.gov

Compare with other makers

Updated May 10, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.