# Innova Corp.

- Location (FDA's records): Washington, DC
- FDA decisions: 6 (1991–2004): 6 510(k) clearances
- Product codes: DZE (4), MQN (1), LYG (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 12 (2 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
- Howmedica Corp.: 1 (https://510kreport.com/company/howmedica)
- Innova Life Sciences Corp.: 1 (https://510kreport.com/company/innova-life-sciences)

## Firms that cite its devices most
- Innova Life Sciences Corp.: 5 (https://510kreport.com/company/innova-life-sciences)
- Ot Medical GmbH: 2 (https://510kreport.com/company/ot-medical)
- GC America, Inc.: 2 (https://510kreport.com/company/gc-america)
- Titan Implants: 1 (https://510kreport.com/company/titan-implants)

## Its most-cited devices
- K971196: Endopore Endosseous Dental Implant System (1997), cited by 7
- K926354: Endo-Pore Endosseous Dental Implant System (1995), cited by 4
- K040714: Hybrid Endopore Endosseous Dental Implant (2004), cited by 1

## Recent decisions
- K040714: Hybrid Endopore Endosseous Dental Implant (Apr 9, 2004)
- K984117: Innova Telescopic Distractor (Feb 10, 1999)
- K971196: Endopore Endosseous Dental Implant System (May 8, 1997)
- K952434: Endopore Dental Implant Abutments (Jul 19, 1995)
- K926354: Endo-Pore Endosseous Dental Implant System (Feb 13, 1995)
- K915361: The Body Buggy (Dec 20, 1991)

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