# Sargon Ent., Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (1994–2010): 3 510(k) clearances
- Product codes: DZE (3)
- Predicates its devices cite: 8 (3 its own); citations of its devices by later devices: 7 (3 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
- Institut Straumann AG: 2 (https://510kreport.com/company/institut-straumann)
- Graham & James: 2 (https://510kreport.com/company/graham-james)
- Straumann USA: 1 (https://510kreport.com/company/straumann-usa)

## Firms that cite its devices most
- Nobel Biocare Uas, Inc.: 2 (https://510kreport.com/company/nobel-biocare-uas)
- Dentack Impants, Ltd.: 1 (https://510kreport.com/company/dentack-impants)
- Straumann USA: 1 (https://510kreport.com/company/straumann-usa)

## Its most-cited devices
- K930071: Sargon Cylindro-Blade Implant (1994), cited by 5
- K981141: Sargon Immediate Load Implant, Model D (1999), cited by 2

## Recent decisions
- K082573: Sargon Non-Expandable Dental Implant (Jul 21, 2010)
- K981141: Sargon Immediate Load Implant, Model D (Jun 23, 1999)
- K930071: Sargon Cylindro-Blade Implant (Jul 8, 1994)

Source page: https://510kreport.com/company/sargon-ent