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KGW

Ring (Wound Protector), Drape Retention, Internal

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)
2
Summaries archived here
2 (direct download)
510(k) clearances (all years, FDA)
9 (all years; only the last 3 years are listed here)

510(k) clearances, last 3 years (2)

Last three years. Most recent: 2026-04-24.

NumberDecision dateApplicantDevice nameSummary
K2609822026-04-24Applied Medical Resources CorporationAlexis lighted wound protector-retractor, flexible, …PDF
K2535312026-02-23Applied Medical Resources CorporationAlexis® Lighted Wound Protector-Retractor, Rigid, Me…PDF

2 summaries are archived here for direct download.

Official FDA classification page: KGW
Classification and pathway per current FDA publications. Data from openFDA (CC0).