BOONE CENTER, INCORPORATED

FDA Device Registration & Listing · Moscow Mills, MO, US · Registration 1937639

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
1937639
FEI Number
1937639
Entity Name
BOONE CENTER, INCORPORATED
City/State/Country
Moscow Mills, MO, US
Establishment Address
245 College Campus Dr, Moscow Mills, MO 63362, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
BOONE CENTER, INC. (Owner Number: 1937639)
Owner / Operator Contact Address
200 TRADE CENTER DR. WEST, --, St Peters, MO 63376, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Oyster Shell

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EHZ Evacuator, Oral Cavity Dental Class 1 872.6640 2013-12-10
EGS Handpiece, Contra- And Right-Angle Attachment, Dental Dental Class 1 872.4200 2013-12-11
LJL Detectors And Removers, Lice, (Including Combs) General Hospital Class 1 880.5960 2022-01-03

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BOONE CENTER, INC.
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 1937639. Last updated year: 2026. Please use registration number 1937639 when referencing this establishment in official correspondence.
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