Educational information only — not medical advice. Individual results vary and no outcome can be guaranteed.

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Accreditation & Regulatory Context

What is regulated, by whom, and how to verify claims independently.

Device regulatory status

The MagDI System (magnetic duodeno-ileostomy device used in Sleeve Plus) is cleared under the U.S. FDA 510(k) pathway for its indicated use. Regulatory status can be verified via the FDA's 510(k) Premarket Notification database. See our references library for source links.

Procedural training

Bariatric and metabolic surgery are performed by surgeons with dedicated fellowship-level training. Ask any surgeon you consult about their case volume, training pathway, and complication rates.

Clinic accreditation

The Obesity Control Center describes itself as an internationally recognized bariatric facility. Institutional accreditation details are OCC-reported; prospective patients are encouraged to verify current accreditation status directly with OCC and with any independent accreditor named at the time of consultation.

How to verify

  • FDA 510(k) database — device clearance status
  • ASMBS "Find a Provider" — surgeon accreditation status (U.S.)
  • IFSO endorsements — international bariatric surgery standards
  • Direct request to the clinic for current documentation

Institutional information on this page is OCC-reported and is not independently audited by SleevePlus.mx.

Last reviewed: June 2026.