GenderBender LLC
Letter data
- Company
- GenderBender LLC
- Recipient
- Xander Shephard | Manager | GenderBender LLC | 21042 S Main St | Carson | , | CA | 90724 | United States | genderbenderapparel@gmail.com
- Issue date
- 2026-03-27
- Posted date
- Not available
- FDA office
- Center for Devices and Radiological Health
- Subject
- Not available
- Product
- Medical Devices
- CMS ID
- 720842
- 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
GenderBender LLC
MARCS-CMS 720842 —
March 27, 2026
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Warning Letters
About Warning and Close-Out Letters
Delivery Method:
VIA Electronic Mail
Product:
Medical Devices
Recipient:
Recipient Name
Xander Shephard
Recipient Title
Manager
GenderBender LLC
21042 S Main St
Carson
,
CA
90724
United States
genderbenderapparel@gmail.com
Issuing Office:
Center for Devices and Radiological Health
United States
Secondary Issuing Offices
United States
Dear Xander Shephard:
The Food and Drug Administration (FDA) has completed an evaluation of GenderBender LLC corrective actions in response to our Warning Letter CMS #720842, dated December 16th, 2025. Based on our evaluation, it appears that you have addressed the violation(s) 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/
Michael J. Hoffmann
Office Director
OHT3: Office of GastroRenal, ObGyn,
General Hospital and Urology Devices
Office of Product Evaluation and Quality
Center for Devices and Radiological Health
Xander Shephard
GenderBender LLC
cc: Shopify, Inc. abuse@shopify.com
cc: gbllcservices@gmail.com
Content current as of:
04/02/2026
Regulated Product(s)
Medical Devices