OHLENDORF COMPANY

FDA Device Registration & Listing · Affton, MO, US · Registration 1000380364

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
1000380364
FEI Number
1000380364
Entity Name
OHLENDORF COMPANY
City/State/Country
Affton, MO, US
Establishment Address
9781 Green Park Industrial Dr, Affton, MO 63123, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
OHLENDORF COMPANY (Owner Number: 9086387)
Owner / Operator Contact Address
9781 Green Park Industrial Dr, --, Saint Louis, MO 63123, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K031809
PMA Number
N/A

All Registered Proprietary Names

Perio Protect Tray

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KMT Tray, Fluoride, Disposable Dental Class 1 872.6870 2006-04-27

Official Correspondent

Kevin OHLENDORF

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OHLENDORF COMPANY
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000380364. Last updated year: 2026. Please use registration number 1000380364 when referencing this establishment in official correspondence.
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