ASCENTCARE DENTAL PRODUCTS

FDA Device Registration & Listing · Grand Haven, MI, US · Registration 3016798774

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016798774
FEI Number
3016798774
Entity Name
ASCENTCARE DENTAL PRODUCTS
City/State/Country
Grand Haven, MI, US
Establishment Address
335 North Griffin, Grand Haven, MI 49417, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Ascentcare Dental Products (Owner Number: 10072763)
Owner / Operator Contact Address
335 North Griffin Street, Grand Haven, MI 49417, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bite Buddy Mouth Prop System Radical Reflector HyperLUX VacuLUX Adapter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EIF Accessories, Retractor, Dental Dental Class 1 872.4565 2020-05-01
EAX Mirror, Mouth Dental Class 1 872.4565 2020-07-16
EAZ Light, Operating, Dental Dental Class 1 872.4630 2021-02-26
EBR Unit, Suction Operatory Dental Class 1 872.6640 2021-02-26

Official Correspondent

Austin Ritter

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ascentcare Dental Products
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016798774. Last updated year: 2026. Please use registration number 3016798774 when referencing this establishment in official correspondence.
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