Class II — Neocis, Inc.
| Recalling firm | Neocis |
|---|---|
| Registered facility | NEOCIS INC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The LRUL and LLUR posterior chairside splints and the LLUR anterior chairside splints may be mislabeled. |
| Product | DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left); accessories to the parent system, the Neocis Guidance System (NGS) |
| Quantity | 100 units |
| Distribution | OH, FL, CT, MA, AZ PA, NY |
| Initiated | 2020-10-30 |
| Classified | 2021-01-26 |
| Terminated | 2021-08-11 |
| Recall number | Z-0929-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Neocis, Inc. (Z-0929-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/87060/
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