FDA Letter API

Edge Biologicals Inc

Letter data

Company
Edge Biologicals Inc
Recipient
Walter C. Edge III | Vice President | Edge Biologicals Inc | 598 N 2nd Street | Memphis | , | TN | 38105-1634 | United States | cal@edgebiological.com
Issue date
2026-02-23
Posted date
Not available
FDA office
Division of Medical Device and Radiological Health Operations Central
Subject
Not available
Product
Medical Devices
CMS ID
660003
Reference number
Not available
FEI
Not available
Inspection dates
Not available

Normalized citations

21 CFR: None found

21 U.S.C.: None found

Related FDA links

No related FDA letter link is present in the source index.

Full source text

CLOSEOUT LETTER Edge Biologicals Inc MARCS-CMS 660003 — February 23, 2026 More Warning Letters Warning Letters About Warning and Close-Out Letters Delivery Method: VIA Electronic Mail Product: Medical Devices Recipient: Recipient Name Walter C. Edge III Recipient Title Vice President Edge Biologicals Inc 598 N 2nd Street Memphis , TN 38105-1634 United States cal@edgebiological.com Issuing Office: Division of Medical Device and Radiological Health Operations Central United States Secondary Issuing Offices United States Dear Mr. Edge: The Food and Drug Administration has completed an evaluation of your firm’s corrective actions in response to our Warning Letter (CMS # 660003, dated June 27, 2023). Based on our evaluation, it appears that you have addressed the violations contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections. This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means. Sincerely, /S/ Barbara C. Marsden Acting Director Office of Regulatory Programs Office of Product Evaluation and Quality Center for Devices and Radiological Health Content current as of: 03/03/2026 Regulated Product(s) Medical Devices