KERANETICS, INC.

FDA Device Registration & Listing · Winston Salem, NC, US · Registration 3015980493

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
3015980493
FEI Number
3015980493
Entity Name
KERANETICS, INC.
City/State/Country
Winston Salem, NC, US
Establishment Address
200 E 1st St Ste 102, Po Box 1, Winston Salem, NC 27101, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
KeraNetics, Inc. (Owner Number: 10061651)
Owner / Operator Contact Address
200 East First Street, Box #4, Suite 102, Winston Salem, NC 27101, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K192386
PMA Number
N/A

All Registered Proprietary Names

KeraStat Cream

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2020-12-09

Official Correspondent

Chiquita Williams

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KeraNetics, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K112888 Kensey Nash Corporation MESO WOUND MATRIX 2012-02-10
K040211 Collagen Matrix, Inc. MODIFICATION TO: COLLAGEN TOPICAL WOUND DRESSING 2004-02-27

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015980493. Last updated year: 2026. Please use registration number 3015980493 when referencing this establishment in official correspondence.
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