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Hanson Medical, Inc.

US

Last updated September 17, 2026

About

Reduce the appearance of surgical, injury, burn, keloid and hypertrophic scars with Scarfade® medical-grade silicone scar gel.

From the manufacturer's own website. Source

What Hanson Medical, Inc. makes

Hanson Medical, Inc. manufactures chin prostheses, nasal cartilage support implants, malar prostheses, silicone-block tissue reconstructive materials, pectoral implants, and scar-management dressings. Specific devices include chin implants, malar implants, nasal dorsal implants, nasal implants, calf implants, gluteal implants, and reusable scar-management dressings.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA UDI registry. Hanson Medical, Inc. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Hanson Medical, Inc. manufacture?

Hanson Medical, Inc. manufactures chin prostheses, nasal cartilage support implants, malar prostheses, silicone-block tissue reconstructive materials, pectoral implants, and scar-management dressings. Specific devices include chin implants, malar implants, nasal dorsal implants, nasal implants, calf implants, gluteal implants, and reusable scar-management dressings.

Where is Hanson Medical, Inc. based?

Hanson Medical, Inc. is based in the United States, as stated in the company's summary and country field.

Which regulatory registries list Hanson Medical, Inc.'s devices?

Hanson Medical, Inc.'s devices are listed in the FDA UDI registry, as indicated in the LISTED IN field and confirmed in the summary.

How are Hanson Medical, Inc.'s devices classified?

Hanson Medical, Inc.'s devices are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field and reiterated in the summary.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
3527 Combine Street, PASO ROBLES, CA, 93446
LinkedIn
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3001890623
DUNS Number
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Catalogue (611)

Page 13 of 13
DeviceModel / ReferenceRegistriesClassStatus
Hanson Scar Ade K040307
FDA 510(k)
Class IActive
Duralastic Anatomical Chin Implants K973575
FDA 510(k)
Class IIActive
Sensei X Robotic Catheter System K141822
FDA 510(k)
Class IIActive
Silicone Carving Block K973728
FDA 510(k)
Class IIActive
Hanson Medical Gluteal Implant K030809
FDA 510(k)
Class IIActive
Duralastic Anatomical Malar Implant K973574
FDA 510(k)
Class IIActive
Powerflex Pec Implant K973729
FDA 510(k)
Class IIActive
Duralastic Anatomical Nasal Implants K973573
FDA 510(k)
Class IIActive
Hanson Medical Facial Implants K090803
FDA 510(k)
Class IIActive
Hanson Medical Calf Implant K030808
FDA 510(k)
Class IIActive
Kelocote Scar Gel And Kelocote Laser Gel K973572
FDA 510(k)
Class IActive

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