# K250967: Sherlock

- Pathway: 510(k) (Traditional)
- Applicant: Open Implants, LLC
- Decided: Jun 26, 2025 after 87 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 20 generations back to K960026 (1996). 359 ancestors in all.
No later device cites it as a predicate yet.
0 of 360 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220482: Sherlock, Open Implants, LLC (2022) Summary page 5.

## Indications for use
Sherlock abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations. All digitally designed CAD/CAM customizations for Sherlock abutments are to be sent to an Open Implants-validated milling center for manufacture. Sherlock abutments are compatible with the implant systems listed in the Compatibility Table:

Source page: https://510kreport.com/device/K250967
Methodology: https://510kreport.com/methodology