# Kinetic Medical Products

- Location (FDA's records): Erie, PA
- FDA decisions: 63 (1989–1989): 63 510(k) clearances
- Product codes: HTD (14), HXD (4), GDF (3), GEG (3), EMF (3), HRR (3), GAD (3), HCZ (3), LRW (2), EMH (2), KNB (1), HCY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Gynex Corp.: 1 (https://510kreport.com/company/gynex)

## Its most-cited devices
- K890379: Uterine Tentaculum (1989), cited by 1

## Recent decisions
- K890385: Midwifery/Obstetrical Forceps (Mar 1, 1989)
- K890387: Malleable Placenta Curette (Feb 27, 1989)
- K890380: Cervical Biopsy Forceps (Feb 27, 1989)
- K890376: Vaginal Speculum (Feb 27, 1989)
- K890382: Compression Forceps (Feb 27, 1989)
- K890216: Microsurgical Keratome (Feb 16, 1989)
- K890383: Hysterectomy Forceps (Feb 16, 1989)
- K890388: Cephalotomy Scissors (Feb 13, 1989)

Source page: https://510kreport.com/company/kinetic-medical-products