# Invivo Corporation (Business Trade Name: Philips)

- Location (FDA's records): Florida, FL
- FDA decisions: 6 (2021–2023): 6 510(k) clearances
- Product codes: MOS (6)
- 510(k) review time since 2016: median 28 days, against 79 for FDA's reviews in the same codes and years (4 of 6 faster)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 5 (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 whose devices it cites most
- Mri Devices Corp.: 3 (https://510kreport.com/company/mri-devices)
- Sentinel Medical, Inc.: 2 (https://510kreport.com/company/sentinel-medical)
- Medical Advances, Inc.: 1 (https://510kreport.com/company/medical-advances)
- Invivo Corporation: 1 (https://510kreport.com/company/invivo)

## Firms that cite its devices most
- Philips Medical Systems Nederland B.V.: 4 (https://510kreport.com/company/philips-medical-systems-nederland)
- Philips Medical System Nederlands B.V.: 1 (https://510kreport.com/company/philips-medical-system-nederlands)

## Its most-cited devices
- K213735: dS Sentinelle Breast 16ch 1.5T Coil (2022), cited by 2
- K222325: 8ch Wrist Coil (2022), cited by 1
- K213727: dS Sentinelle Breast 16ch 3.0T Coil (2022), cited by 1
- K232762: dS Breast Coil 7ch 1.5T (2023), cited by 1

## Recent decisions
- K232762: dS Breast Coil 7ch 1.5T (Oct 3, 2023)
- K222325: 8ch Wrist Coil (Aug 31, 2022)
- K222257: 1.5 T/R Quad Extremity Coil, 1.5T 8CH T/R Knee Coil (Aug 23, 2022)
- K213735: dS Sentinelle Breast 16ch 1.5T Coil (Aug 8, 2022)
- K213727: dS Sentinelle Breast 16ch 3.0T Coil (Aug 8, 2022)
- K213351: ds Head 32ch 3.0T (Oct 29, 2021)

Source page: https://510kreport.com/company/invivo-business-trade-name-philips