# Sybron Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 37 (1977–1986): 37 510(k) clearances
- Product codes: GEI (4), FRC (2), EMA (2), ELW (2), DXN (2), EBF (2), JOJ (1), JTQ (1), DZN (1), FLI (1), DXT (1), KQS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (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
- Senorx, Inc.: 3 (https://510kreport.com/company/senorx)
- Getinge/Castle, Inc.: 2 (https://510kreport.com/company/getinge-castle)
- Vivant Medical, Inc.: 2 (https://510kreport.com/company/vivant-medical)
- New Stetic: 1 (https://510kreport.com/company/new-stetic)
- Mdt Biologic Co.: 1 (https://510kreport.com/company/mdt-biologic)
- Foremost Dental Mfg., Inc.: 1 (https://510kreport.com/company/foremost-dental-mfg)
- Sybron Dental Specialties, Inc.: 1 (https://510kreport.com/company/sybron-dental-specialties)

## Its most-cited devices
- K790187: Bovie Hand Control (1979), cited by 5
- K820783: Castle Microcomputer Sterilizer Control (1982), cited by 3
- K841910: Kerr Sealapex Root Canal Sealer (1984), cited by 1
- K820181: Sybron/Kerr Contour (1982), cited by 1
- K862284: Sealite (1986), cited by 1

## Recent decisions
- K862284: Sealite (Jun 23, 1986)
- K854855: Proof Alginate Impression Material (Jan 30, 1986)
- K844092: Diagnostic Microsopce Slides (Oct 25, 1984)
- K842132: Tycos Self-Check/Digital Fever Thermo (Jul 18, 1984)
- K841910: Kerr Sealapex Root Canal Sealer (Jul 13, 1984)
- K841732: Liebel-Flarsheim Afc 1000 X-Ray Film (Jun 5, 1984)
- K840469: Tycos Self Check BPM3 Blood Press Moni (May 21, 1984)
- K840407: Kerr Resin Bonded Bridge Cement (May 21, 1984)

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