# Evermed, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 9 (1983–2002): 9 510(k) clearances
- Names in FDA's records: Evermed, Inc. (6); Evermed Corp. (3)
- Product codes: LJS (4), IOR (2), DRC (1), FKX (1), ITI (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Sunrise Medical, Inc.: 1 (https://510kreport.com/company/sunrise-medical)
- Invacare Corp.: 1 (https://510kreport.com/company/invacare)
- Gendron, Inc.: 1 (https://510kreport.com/company/gendron)

## Firms that cite its devices most
- C.R. Bard, Inc.: 2 (https://510kreport.com/company/cr-bard)
- American Bantex Corp.: 1 (https://510kreport.com/company/american-bantex)

## Its most-cited devices
- K830256: Non-Sterile Broviac Parenteral Alimi- (1983), cited by 1
- K830233: Non-Sterile,Single/Souble Lumen-Cath (1983), cited by 1
- K023485: Explorer Powered Wheelchair (2002), cited by 1

## Recent decisions
- K023993: Galaxy Series Wheelchair (Dec 27, 2002)
- K024030: Millennium Series Manual Wheelchairs (Dec 12, 2002)
- K023485: Explorer Powered Wheelchair (Dec 2, 2002)
- K840846: Sterile Hichman/Broviac Injection Cap (Jul 6, 1984)
- K840529: Steiger Tunneling Instrument 285 (Mar 12, 1984)
- K830256: Non-Sterile Broviac Parenteral Alimi- (Mar 1, 1983)
- K830406: Non-Sterile Catheter Repair Kits (Mar 1, 1983)
- K830233: Non-Sterile,Single/Souble Lumen-Cath (Feb 28, 1983)

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