# American Medical Devices, Inc.

- Location (FDA's records): Atlanta, GA
- FDA decisions: 6 (1997–1998): 6 510(k) clearances
- Product codes: MPA (3), HJK (1), KYG (1), HMX (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Ocular Instruments, Inc.: 1 (https://510kreport.com/company/ocular-instruments)

## Firms that cite its devices most
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Iscience Surgical Corporation: 1 (https://510kreport.com/company/iscience-surgical)
- Iscience Interventional: 1 (https://510kreport.com/company/iscience-interventional)

## Its most-cited devices
- K970882: Endolight End Irrigating Endo-Illuminator (20 GA. and 19 GA.) (1997), cited by 3

## Recent decisions
- K974561: Moistair Fluid Air Tubing Set (Feb 19, 1998)
- K971853: Endoview Spphire Lens Set (Aug 6, 1997)
- K970882: Endolight End Irrigating Endo-Illuminator (20 GA. and 19 GA.) (Jun 24, 1997)
- K970875: Endolight Fiberoptic Endo-Illuminator (20 GA. & 19 GA.) (May 20, 1997)
- K970873: Endosoft Soft Tip Needle (20 GA. and 19 GA.) (May 20, 1997)
- K970878: Endolight Fiberoptic Regular Monofilament and Fine Monofilament (May 6, 1997)

Source page: https://510kreport.com/company/american-medical-devices