# Generic Medical Device, Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 4 (2007–2011): 4 510(k) clearances
- Product codes: OTN (2), FTL (1), HFX (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- ETHICON, Inc.: 2 (https://510kreport.com/company/ethicon)
- Generic Medical Devices, Inc.: 1 (https://510kreport.com/company/generic-medical-devices)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Caldera Medical, Inc.: 1 (https://510kreport.com/company/caldera-medical)
- Zinnanti Surgical Instruments, Inc.: 1 (https://510kreport.com/company/zinnanti-surgical-instruments)

## Firms that cite its devices most
- Neomedic International S.L.: 1 (https://510kreport.com/company/neomedic-international)
- Generic Medical Devices, Inc.: 1 (https://510kreport.com/company/generic-medical-devices)

## Its most-cited devices
- K083471: GMD Universal Sling, Model Product Code 1010 and 1020 (2009), cited by 3

## Recent decisions
- K111219: GMD Universal Urinary Incontinence Sling (Jun 30, 2011)
- K083471: GMD Universal Sling, Model Product Code 1010 and 1020 (Mar 3, 2009)
- K070018: Universal Surgical Mesh, Model 100 (Apr 27, 2007)
- K063429: GMD Universal Circumcision Clamp, Model 200 (Jan 17, 2007)

Source page: https://510kreport.com/company/generic-medical-device