# Teknar, Inc.

- Location (FDA's records): Fenton, MO
- FDA decisions: 18 (1980–1990): 18 510(k) clearances
- Product codes: IYO (9), ITX (1), EPT (1), FSO (1), HQC (1), HPY (1), FCG (1), HDR (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 10 (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
- Amertek Medical, Inc.: 3 (https://510kreport.com/company/amertek-medical)
- Accutome, Inc.: 2 (https://510kreport.com/company/accutome)
- Mentor Ophthalmics, Inc.: 1 (https://510kreport.com/company/mentor-ophthalmics)
- Envisioneering, LLC: 1 (https://510kreport.com/company/envisioneering)
- Devmed Corp.: 1 (https://510kreport.com/company/devmed)
- Alton Design, LLC: 1 (https://510kreport.com/company/alton-design)
- Tayman Medical, Inc.: 1 (https://510kreport.com/company/tayman-medical)

## Its most-cited devices
- K864807: Teknar Proscan (TM) (1987), cited by 5
- K881605: Biopsy Guide (1988), cited by 2
- K860757: Ophthasonic a-Scan (1986), cited by 1
- K903666: Ophthasonic a/P Iii (1990), cited by 1
- K871536: Ophthasonic a-Scan/ B-Scan (1987), cited by 1

## Recent decisions
- K903666: Ophthasonic a/P Iii (Nov 19, 1990)
- K896038: B-Scan 10 MHZ Probe (Apr 23, 1990)
- K896150: Image 2000 System, Imaging, Ultra-Sonic (Jan 18, 1990)
- K891777: Pro-Cut Biopsy Needle (May 4, 1989)
- K883965: Probe, Imaging, Ultrasonic, Mechanical Sector (Oct 5, 1988)
- K881850: Teknar Percu-Scan (Aug 29, 1988)
- K881605: Biopsy Guide (Jun 21, 1988)
- K880659: Teknar Proscan Accessory Probe (Apr 14, 1988)

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