Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Open, Classified

BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic appliance, typically supplied in series intended to be worn in succession and self-changed every few weeks, designed to influence the shape and/or function of the stomatognathic system to correct malocclusions.

FDA Recall Z-0750-2025 · Posted 2024-12-23

Recalling FirmStraight Smile, LLC
Recall StatusOpen, Classified
Product CodeNXC
Date Initiated2024-11-04
Product Quantity5,324,178 devices

Reason for Recall

Virtual-only clinical workflow utilized for dental aligners and impression to approve patients for aligner devices may not be suitable for patients who have certain contraindications.

Firm Action

On 11/04/2024 and 11/07/2024, the firm sent an "URGENT: MEDICAL DEVICE CORRECTION" Letter via email to customers informing them of the potential risks associated with BYTE Aligners that the patient onboarding workflow may not provide adequate assurance that patients with active periodontal disease, severe open bite, severe overjet, tooth malocclusion requiring surgical correction, mixed dentition, dental prosthetics or dental implants, or adolescents with skeletally narrow jaws do not enter treatment with BYTE Aligners. The BYTE workflow may not be adequate to identify the conditions for which BYTE Aligners are contraindicated because an in-person exam is not performed. This means that potential patients with one of the above issues may not be appropriately filtered out from treatment. For customers who are actively in treatment. To minimize the risk of illness or injury, we recommend the following: For customers who knowingly suffer from active periodontal disease, severe open bite, severe overjet, tooth malocclusion requiring surgical correction, mixed dentition, have dental prosthetics or dental implants, or are an adolescent with a skeletally narrow jaw, discontinue aligner treatment immediately and visit a dental professional. For all other customers, please promptly visit a dental professional to confirm whether continuing aligner treatment is appropriate for you. Following your dentist visit, please visit https://patient.byte.com/support to upload (i) the name and contact information for the dental professional you visited, (ii) the date visited, and (iii) any visit notes provided by the dental professional during your visit. BYTE will reach out to you to gather a signed consent to enable us to gather other information needed from such dental professional. For questions/concerns - contact treating dentist by submitting a support request through Patient Account Center (https://patient.byte.com/support), the My Byte App, or calling Byte support (877) 298-36

Root Cause

Device Design

Distribution Pattern

Worldwide - U.S. Nationwide distribution including in the states of CO, KS, MI, IL, GA NY, MN, IN, PA, TX, NJ, MS, RI, SD, FL, KY, CA, OR, WI, WY, MA, NC, WA, AR, UT, OH, SC, NM, CT, TN, LA, NE, AL, MO, VA, MD, IA, OK, NV, DE, VT, AZ, RI, HI, WV, NH, MT, AK, ID, Puerto Rico, ME and the countries of Australia.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑