# Bofors Nobelpharma, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1982–1984): 3 510(k) clearances
- Product codes: DZE (2), ERL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (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
- Oraltronics Marketing-Und Vertriebs GmbH: 2 (https://510kreport.com/company/oraltronics-marketing-und-vertriebs)
- Crystal Medical Technology: 1 (https://510kreport.com/company/crystal-medical-technology)
- Quantum Bioengineering, Ltd.: 1 (https://510kreport.com/company/quantum-bioengineering)
- Dentatus USA, Ltd.: 1 (https://510kreport.com/company/dentatus-usa)

## Its most-cited devices
- K820013: Titanium Implant Devices (1982), cited by 4
- K841551: Osseointegrated Fixtures-Tissue Integr (1984), cited by 1

## Recent decisions
- K841813: Tissue Integrated Prosthesis Drill (Aug 10, 1984)
- K841551: Osseointegrated Fixtures-Tissue Integr (Jun 22, 1984)
- K820013: Titanium Implant Devices (Mar 1, 1982)

Source page: https://510kreport.com/company/bofors-nobelpharma