KGW
- Product code
- KGW
- Device name
- Ring (Wound Protector), Drape Retention, Internal
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.4370
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 9
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K260982 | 2026-04-24 | Applied Medical Resources Corporation | Alexis lighted wound protector-retractor, flexible, | |
| K253531 | 2026-02-23 | Applied Medical Resources Corporation | Alexis® Lighted Wound Protector-Retractor, Rigid, Me |
Official FDA classification page: KGW
Classification and pathway per current FDA publications. Data from openFDA (CC0).