# Xtremi-T, LLC

- Location (FDA's records): Lawrenceville, NJ
- FDA decisions: 2 (2005–2005): 2 510(k) clearances
- Product codes: HWC (1), HTY (1)
- Predicates its devices cite: 23 (0 its own); citations of its devices by later devices: 1 (0 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
- Bionx Implants, Inc.: 7 (https://510kreport.com/company/bionx-implants)
- Biomet, Inc.: 4 (https://510kreport.com/company/biomet)
- Inion, Ltd.: 3 (https://510kreport.com/company/inion)
- Linvatec Biomaterials, Ltd.: 2 (https://510kreport.com/company/linvatec-biomaterials)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)
- Bioscience, Inc.: 1 (https://510kreport.com/company/bioscience)
- Arthrotek, Inc.: 1 (https://510kreport.com/company/arthrotek)

## Firms that cite its devices most
- Bio2 Technologies, Inc.: 1 (https://510kreport.com/company/bio2-technologies)

## Its most-cited devices
- K043339: Refix Pin (Plla), Models 2070L, 2770L, 3570L, 4570L; (Plga), Models 2070LG, 2770LG, 3570LG, 4570LG (2005), cited by 1

## Recent decisions
- K050388: Refix Internal Fracture Fixation Screws (Sep 7, 2005)
- K043339: Refix Pin (Plla), Models 2070L, 2770L, 3570L, 4570L; (Plga), Models 2070LG, 2770LG, 3570LG, 4570LG (Apr 18, 2005)

Source page: https://510kreport.com/company/xtremi-t