# Gi Supply

- Location (FDA's records): Camp Hill, PA
- FDA decisions: 10 (1992–2023): 10 510(k) clearances
- Names in FDA's records: Gi Supply (8); Gi Supply, Inc. (2)
- Product codes: PLL (2), LYR (2), BTA (2), LRO (1), MNK (1), FGE (1), EOQ (1)
- 510(k) review time since 2016: median 338 days, against 280 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 6 (3 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cosmo Technologies, Ltd.: 1 (https://510kreport.com/company/cosmo-technologies)

## Firms that cite its devices most
- Oridion Medical 1987, Ltd.: 2 (https://510kreport.com/company/oridion-medical-1987)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)

## Its most-cited devices
- K970186: GI Supply Paracentesis Pump (1997), cited by 2
- K191923: EverLift Submucosal Lifting Agent (2020), cited by 1
- K970187: Runyon Large Volume Paracentesis Kit (1997), cited by 1
- K931044: Oxy-Bloc (1993), cited by 1
- K915816: Bite Block/Mouthpiece for Endoscopy (1992), cited by 1

## Recent decisions
- K221042: Renova RP Centesis Pump (Apr 19, 2023)
- K202376: EverLift Submucosal Lifting Agent (Sep 30, 2020)
- K191923: EverLift Submucosal Lifting Agent (Jun 20, 2020)
- K031360: GI Supply Biliary Stent (Sep 24, 2003)
- K012411: HP-ONE (Sep 25, 2001)
- K970187: Runyon Large Volume Paracentesis Kit (Feb 14, 1997)
- K970186: GI Supply Paracentesis Pump (Feb 14, 1997)
- K944903: HP-Fast (Apr 20, 1995)

Source page: https://510kreport.com/company/gi-supply