Ortho Organizers, Inc.
Ortho Organizers, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2025, with 2 FDA device recalls on record.
Top product codes for Ortho Organizers, Inc.
FDA recalls by Ortho Organizers, Inc.
- Z-2477-2020 — Maestro Orthodontic Bracket REF711-206-10 QTY. 10 Rx Only (01)00190707016517 (10)112233 (422)484
- Z-2478-2020 — Maestro Orthodontic Bracket REF711-298Q QTY. 20 Rx Only (01)00190707017064 (10)889437 (422)484 Maestro Orthodontic Bracket REF711-299MCQ QTY. 20 Rx Only (01)00190707017071(10)889437 (422)484
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Ortho Organizers, Inc.
- K252760 — Carriere® Motion Pro® Clear Bite Corrector
- K173440 — Carriere SLX 3D Clear
- K160720 — Carriere Motion Clear Class II
- K110335 — CERAMIC BRACKETS
- K061266 — ORTHO ORGANIZERS TEMPORARY ORTHODONTIC ANCHOR
- K923218 — NITANIUM PALATAL EXPANDER
- K931980 — STAINLESS STEEL ORTHODONTIC PRODUCTS
- K931663 — NITANIUM PRO FORM ARCHWIRES,ROUND,SQUARE,RECTANGUL
Data sourced from openFDA. This site is unofficial and independent of the FDA.