KGE
- Product code
- KGE
- Device name
- Forceps, Biopsy, Electric
- Device class
- Class 2
- 21 CFR
- 21 CFR 876.4300
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 4
- Summaries archived here
- 4 (direct download)
- 510(k) clearances (all years, FDA)
- 46 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (4)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K251807 | 2026-03-06 | Olympus Medical Systems Corp. | Single Use Electrosurgical Hemostatic Forceps FD-410… | |
| K250187 | 2025-10-07 | Olympus Medical Systems Corporation | Disposable Hot Biopsy Forceps (FD-210U); Disposable … | |
| K242857 | 2025-05-21 | Finemedix Co., Ltd. | ClearHemograsper | |
| K231721 | 2023-12-14 | Beijing Zksk Technology Co., Ltd. | Disposable Hot Biopsy Forceps |
Official FDA classification page: KGE
Classification and pathway per current FDA publications. Data from openFDA (CC0).