# Sterling Drug, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 9 (1978–1990): 9 510(k) clearances
- Product codes: LYC (3), KGN (2), DZE (1), FMI (1), JTQ (1), FMF (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
- Organogenesis, Inc.: 1 (https://510kreport.com/company/organogenesis)
- Hospira, Inc.: 1 (https://510kreport.com/company/hospira)
- Biogen: 1 (https://510kreport.com/company/biogen)
- Nordson Efd: 1 (https://510kreport.com/company/nordson-efd)
- Integra LifeSciences Corporation: 1 (https://510kreport.com/company/integra-lifesciences)
- Shandong Weigao Group Medical Polymer Co., Ltd.: 1 (https://510kreport.com/company/shandong-weigao-group-medical-polymer)
- Smith & Nephew Medical Limited: 1 (https://510kreport.com/company/smith-nephew-medical)

## Its most-cited devices
- K820164: Empty Sterile Carpuject (1982), cited by 4
- K901369: Green Label Biobrane II and Red Label Biobrane II (1990), cited by 2
- K896110: Biobrane (R) II (1989), cited by 1

## Recent decisions
- K901369: Green Label Biobrane II and Red Label Biobrane II (Jun 5, 1990)
- K896110: Biobrane (R) II (Nov 28, 1989)
- K875275: Winthrop Pharmaceuticals Contrast Media Warmer (Jan 27, 1988)
- K840260: Periograf Durapatite 40-60 Mesh (Apr 5, 1984)
- K820023: Conagraf TM Durapatite Cones (Feb 24, 1982)
- K820164: Empty Sterile Carpuject (Feb 24, 1982)
- K813257: Alveograf Durapatite (18-40 Mesh) (Jan 5, 1982)
- K813070: Periograf (Nov 20, 1981)

Source page: https://510kreport.com/company/sterling-drug