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Pillar Surgical, Inc.

Also registered as Pillar Surgical

United StatesFDA applicant, unverified

Devices
7

What Pillar Surgical, Inc. makes

Pillar Surgical, Inc. manufactures synthetic facial and chest implants for cosmetic augmentation, including chin, nasal, malar (cheek), and pectoral implants. Their product line also includes pre-shaped contour carving blocks for customised implant shaping in facial reconstruction procedures.

The company’s devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. Implants are listed in the FDA’s 510(k) database, reflecting their compliance with US medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Pillar Surgical, Inc. have in the registry?

The registry currently lists 7 devices for Pillar Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Pillar Surgical, Inc.'s devices?

Among its 7 most recently registered devices, Pillar Surgical, Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Pillar Surgical, Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Pillar Surgical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Pillar Surgical, Inc. in the registry?

The most recently registered devices listed for Pillar Surgical, Inc. include PILLAR CHIN IMPLANT, SILMAX CONTOUR CARVING BLOCK IMPLANT, PROLASTIC SHEETING and PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS.

Generated automatically from registry data and not verified by a human reviewer.