Skip to content

Aesthetic and Reconstructive Technologies, Inc.

United StatesFDA applicant, unverified

Devices
10

What Aesthetic and Reconstructive Technologies, Inc. makes

The company manufactures silicone-based implants and surgical materials for aesthetic and reconstructive procedures, including nasal, chin, malar, pectoralis, and gluteal implants. It also produces silicone sheeting, tubing, and carving blocks for custom implant fabrication, alongside a silicone gel designed for scar management.

These devices are classified under FDA regulations as Class I and Class II, with most requiring 510(k) clearance. The company’s products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

  • Aart Silicone Sheeting Ref K022223

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Aart Silicone Tubing Ref K022306

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Aart Calf Implant Ref K022511 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Aart Nasal Implant Ref K021418

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Dimisil Scar Gel Ref K023678

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Aart Chin Implant Ref K021417 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Aart Pectoralis Implant Ref K021337 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Aart Silicone Carving Block Ref K021820 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Aart Malar Implant Ref K021419 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Aart Gluteal Implant Ref K021839 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Aesthetic and Reconstructive Technologies, Inc. have in the registry?

The registry currently lists 10 devices for Aesthetic and Reconstructive Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aesthetic and Reconstructive Technologies, Inc.'s devices?

Among its 10 most recently registered devices, Aesthetic and Reconstructive Technologies, Inc. has devices listed in FDA 510(k) (10 devices).

What risk classes do Aesthetic and Reconstructive Technologies, Inc.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Aesthetic and Reconstructive Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Aesthetic and Reconstructive Technologies, Inc. in the registry?

The most recently registered devices listed for Aesthetic and Reconstructive Technologies, Inc. include AART SILICONE SHEETING, AART SILICONE TUBING, AART CALF IMPLANT and AART NASAL IMPLANT.

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