KLANN, INC.

FDA Device Registration & Listing · WAYNESBORO, VA, US · Registration 1123223

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
1123223
FEI Number
1000123102
Entity Name
KLANN, INC.
City/State/Country
WAYNESBORO, VA, US
Establishment Address
301 FOURTH ST., WAYNESBORO, VA 22980, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Klann, Inc (Owner Number: 9009318)
Owner / Operator Contact Address
301 FOURTH ST., --, Waynesboro, VA 22980, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Provale Cup DermaBlade

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILC Utensil, Eating Physical Medicine Class 1 890.5050 2018-08-20
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2014-05-02

Official Correspondent

Debbie Meadows

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Klann, 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 1123223. Last updated year: 2026. Please use registration number 1123223 when referencing this establishment in official correspondence.
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