# Li Medical Technologies, Inc.

- Location (FDA's records): Shelton, CT
- FDA decisions: 17 (1993–2000): 17 510(k) clearances
- Product codes: MBI (7), MAI (4), GCJ (2), HWC (2), JDR (1), HRX (1)
- Predicates its devices cite: 28 (18 its own); citations of its devices by later devices: 22 (18 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
- Mitek Surgical Products, Inc.: 9 (https://510kreport.com/company/mitek-surgical-products)
- ETHICON, Inc.: 1 (https://510kreport.com/company/ethicon)

## Firms that cite its devices most
- Linvatec Corp.: 3 (https://510kreport.com/company/linvatec)
- Suspension Orthopaedic Solutions, LLC: 1 (https://510kreport.com/company/suspension-orthopaedic-solutions)

## Its most-cited devices
- K951233: LMT Bone Anchor (1995), cited by 5
- K960825: LM Anchor or Other Proprietary Name (1996), cited by 3
- K951472: LMT Bone Anchor (1995), cited by 2
- K983435: Rotorblade (1999), cited by 2
- K953764: LMT Bone Anchor (1995), cited by 2
- K963812: LM Bone Anchor (Orthopedics) (1996), cited by 2

## Recent decisions
- K002413: Ultrasorb Suture Anchor (Sep 19, 2000)
- K993373: Rotorblade Suture Anchor (Oct 27, 1999)
- K992938: Rotorblade Suture Anchor (Sep 23, 1999)
- K983435: Rotorblade (Apr 29, 1999)
- K981764: LM Anchor (Jul 13, 1998)
- K981755: LM Anchor (Jul 13, 1998)
- K963288: LM Bone Anchor (Nov 13, 1996)
- K963812: LM Bone Anchor (Orthopedics) (Nov 12, 1996)

Source page: https://510kreport.com/company/li-medical-technologies