# OrthoGrid Systems, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 4 (2019–2026): 4 510(k) clearances
- Product codes: LLZ (3), QIH (1)
- 510(k) review time since 2016: median 122 days, against 112 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 5 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Jointpoint, Inc.: 1 (https://510kreport.com/company/jointpoint)

## Firms that cite its devices most
- Metamorphosis GmbH: 1 (https://510kreport.com/company/metamorphosis)
- Orthopedic Driven Imaging, LLC: 1 (https://510kreport.com/company/orthopedic-driven-imaging)

## Its most-cited devices
- K210136: PhantomMSK Hip (2021), cited by 3
- K182332: PhantomMSK (2019), cited by 2

## Recent decisions
- K260077: OrthoGrid Hip AI® 4.0 (May 29, 2026)
- K210136: PhantomMSK Hip (Feb 18, 2021)
- K192279: PhantomMSK Trauma (Dec 7, 2019)
- K182332: PhantomMSK (Feb 15, 2019)

Source page: https://510kreport.com/company/orthogrid-systems