# Laurimed, LLC

- Location (FDA's records): Redwood City, CA
- FDA decisions: 8 (2008–2017): 8 510(k) clearances
- Product codes: ERL (3), BSP (3), HRX (2)
- Predicates its devices cite: 13 (5 its own); citations of its devices by later devices: 5 (5 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
- Medtronic Xomed, Inc.: 2 (https://510kreport.com/company/medtronic-xomed)
- Surgical Dynamics, Inc.: 2 (https://510kreport.com/company/surgical-dynamics)
- Epimed International, Inc.: 1 (https://510kreport.com/company/epimed-international)
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)
- Pajunk GmbH: 1 (https://510kreport.com/company/pajunk)
- Smiths Medical Asd, Inc.: 1 (https://510kreport.com/company/smiths-medical-asd)

## Its most-cited devices
- K133133: Laurimed Polypvac Microdebrider (2013), cited by 1
- K083909: Spinal Injection System (2009), cited by 1
- K080140: Laurimed Spinal Injection System (2008), cited by 1
- K082194: Laurimed Percutaneous Discectomy System, Model FG-000002 (2008), cited by 1
- K161101: PolypVac Microdebrider (3.3mm and 4.0mm) (2016), cited by 1

## Recent decisions
- K163247: 3.3 mm Laurimed Microdebrider; 4.0 mm Laurimed Microdebrider (Mar 9, 2017)
- K161101: PolypVac Microdebrider (3.3mm and 4.0mm) (Jun 22, 2016)
- K133133: Laurimed Polypvac Microdebrider (Dec 23, 2013)
- K091818: Laurimed Spinal Injection System (Sep 23, 2009)
- K090815: Percutaneous Discectomy System (May 21, 2009)
- K083909: Spinal Injection System (Mar 18, 2009)
- K082194: Laurimed Percutaneous Discectomy System, Model FG-000002 (Aug 28, 2008)
- K080140: Laurimed Spinal Injection System (May 9, 2008)

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