# Gtimd, LLC

- Location (FDA's records): Amherst, NH
- FDA decisions: 3 (2016–2021): 3 510(k) clearances
- Product codes: PON (3)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medicem Technology S.R.O: 1 (https://510kreport.com/company/medicem-technology)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)

## Firms that cite its devices most
- Crossbay Medical, Inc.: 1 (https://510kreport.com/company/crossbay-medical)

## Its most-cited devices
- K160664: Aqueduct 100 Cervical Dilator (2016), cited by 3

## Recent decisions
- K202433: Aqueduct 200 Cervical Dilation Balloon Catheter (Oct 15, 2021)
- K202427: Aqueduct 100 Plus Cervical Dilation Balloon Catheter (Nov 6, 2020)
- K160664: Aqueduct 100 Cervical Dilator (Aug 1, 2016)

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