# Gynescope Corp.

- Location (FDA's records): Willoughby, OH
- FDA decisions: 9 (1990–1990): 9 510(k) clearances
- Product codes: HET (4), HFB (1), HDF (1), HIF (1), KNF (1), EJT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K902657: Gynescope Laparoscopic Forceps (Sep 19, 1990)
- K902658: Gynescope Monopolar Forceps and Electrodes (Sep 19, 1990)
- K901530: Wallace Intrauterine Insemination Catheter (Jul 23, 1990)
- K902655: Gynescope Laparoscopes (Jul 13, 1990)
- K902656: Gynescope Laparoscopic Trocars and Sleeves (Jun 29, 1990)
- K902049: Croak Ovarian Biopsy Forcep (Jun 7, 1990)
- K902019: Modified Metal Speculum & Special Bullet Forceps (Jun 7, 1990)
- K900878: Ott Insufflation Filter Tubing (May 7, 1990)

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