# Interscope, Inc.

- Location (FDA's records): Whitinsville, MA
- FDA decisions: 4 (2017–2020): 3 510(k) clearances and 1 De Novo grant
- Product codes: PTE (2), ERL (1), QNE (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 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
- Medtronic Xomed, Inc.: 1 (https://510kreport.com/company/medtronic-xomed)
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)

## Its most-cited devices
- K170120: EndoRotor (2017), cited by 1

## Recent decisions
- DEN200016: EndoRotor Device (Dec 23, 2020)
- K190715: EndoRotor Console, EndoRotor Catheter, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Roll Stand (Dec 13, 2019)
- K181127: EndoRotor Console, EndoRotor Catheters, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Foot Control (Jan 3, 2019)
- K170120: EndoRotor (Apr 18, 2017)

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