# Sunmed, Inc.

- Location (FDA's records): Redding, CA
- FDA decisions: 7 (1993–2024): 7 510(k) clearances
- Names in FDA's records: Sunmed, Inc. (4); Sunmed, LLC (2); Sunmed (1)
- Product codes: LZN (2), BXN (1), CCW (1), BSK (1), EZL (1), IPF (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 6 (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
- Life-Tech Intl., Inc.: 1 (https://510kreport.com/company/life-tech-intl)
- Posey Co.: 1 (https://510kreport.com/company/posey)
- Rusch Intl.: 1 (https://510kreport.com/company/rusch-intl)
- Rusch, Inc.: 1 (https://510kreport.com/company/rusch)
- Digitimer, Ltd.: 1 (https://510kreport.com/company/digitimer)

## Firms that cite its devices most
- Exactech, Inc.: 2 (https://510kreport.com/company/exactech)
- Joan Spiegel, MD: 1 (https://510kreport.com/company/joan-spiegel-md)
- Hospitech Respiration, Ltd.: 1 (https://510kreport.com/company/hospitech-respiration)
- Easy Med Instrument Co., Ltd.: 1 (https://510kreport.com/company/easy-med-instrument)
- Arm Medical Devices, Inc.: 1 (https://510kreport.com/company/arm-medical-devices)

## Its most-cited devices
- K081805: Cuffalert (2008), cited by 3
- K955632: Orthoplug Soft Bone Design (1996), cited by 1
- K121743: Easymed Peripheral Nerve Stimulator-Sunstin (2013), cited by 1
- K955631: Orthoplug Hard Bone Design (1996), cited by 1

## Recent decisions
- K233098: MYOTouch Muscle Stimulator (Aug 2, 2024)
- K121743: Easymed Peripheral Nerve Stimulator-Sunstin (Mar 28, 2013)
- K081805: Cuffalert (Nov 14, 2008)
- K062112: Sunmed Foley Catheters (Jun 4, 2007)
- K955632: Orthoplug Soft Bone Design (Feb 27, 1996)
- K955631: Orthoplug Hard Bone Design (Feb 27, 1996)
- K921263: Sunlite Laryngoscope (Jun 1, 1993)

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