# J.F. Jelenko & Co., Inc.

- Location (FDA's records): Armonk, NY
- FDA decisions: 56 (1988–2001): 56 510(k) clearances
- Names in FDA's records: J.F. Jelenko & Co., Inc. (55); J.F. Jelenko & Co. (1)
- Product codes: EJT (38), EJS (11), EIH (2), EBG (1), EJJ (1), EBI (1), ELM (1), EBF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (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
- Sterngold: 3 (https://510kreport.com/company/sterngold)
- Sb Lucius, Inc.: 2 (https://510kreport.com/company/sb-lucius)
- Heraeus Kulzer, Inc.: 1 (https://510kreport.com/company/heraeus-kulzer)
- Wieland Edelmetalle GmbH & Co.: 1 (https://510kreport.com/company/wieland-edelmetalle)

## Its most-cited devices
- K001196: Jel Bios 90 (Code Name RD-2401) (2000), cited by 1
- K944679: JEL 96 (1994), cited by 1
- K002645: Jel Bios Pure (2000), cited by 1
- K923720: Suncast (1993), cited by 1
- K923714: Symphony (1993), cited by 1
- K944887: Eureka Plus (1994), cited by 1

## Recent decisions
- K012303: JEL-20 (Aug 22, 2001)
- K002993: Heraceram (Nov 16, 2000)
- K002645: Jel Bios Pure (Oct 19, 2000)
- K002222: RD-2104 (Aug 31, 2000)
- K001360: Signum (Jun 20, 2000)
- K001260: Allround 55 LF (May 17, 2000)
- K001196: Jel Bios 90 (Code Name RD-2401) (May 11, 2000)
- K000532: JEL 15 (Apr 6, 2000)

Source page: https://510kreport.com/company/jf-jelenko