# LinkBio Corp.

- Location (FDA's records): Dover, NJ
- FDA decisions: 2 (2019–2025): 2 510(k) clearances
- Product codes: QHE (1), KRO (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Waldemar Link GmbH & Co. KG: 3 (https://510kreport.com/company/waldemar-link)
- Cleveland Clinic: 1 (https://510kreport.com/company/cleveland-clinic)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)

## Recent decisions
- K241470: CORE Shoulder System (Feb 20, 2025)
- K190181: Instruments for LINK MEGASYSTEM-C Family (Oct 25, 2019)

Source page: https://510kreport.com/company/linkbio