DRI-ANGLE INC

FDA Device Registration & Listing · Niagara Falls, NY, US · Registration 3015192281

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
3015192281
FEI Number
3015192281
Entity Name
DRI-ANGLE INC
City/State/Country
Niagara Falls, NY, US
Establishment Address
4600 Witmer Industrial Estates Rd, Unit 8, Niagara Falls, NY 14305, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Dri-Angle Inc (Owner Number: 10059493)
Owner / Operator Contact Address
4600 Witmer Industrial Estates Rd, Unit 8, Niagara Falls, NY 14305, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dri-Angle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KHR Absorber, Saliva, Paper Dental Class 1 872.6050 2019-01-29

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dri-Angle 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 3015192281. Last updated year: 2026. Please use registration number 3015192281 when referencing this establishment in official correspondence.
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