# Invivo Corporation

- Location (FDA's records): Florida, FL
- FDA decisions: 39 (2005–2021): 39 510(k) clearances
- Names in FDA's records: Invivo Corporation (29); Invivo (6); Invivo Corp. (4)
- Product codes: MOS (21), MWI (8), LLZ (7), MHX (2), DQA (1)
- 510(k) review time since 2016: median 36 days, against 106 for FDA's reviews in the same codes and years (7 of 8 faster)
- Predicates its devices cite: 45 (18 its own); citations of its devices by later devices: 47 (18 its own)
- Recalls linked to its devices: 25 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mri Devices Corp.: 5 (https://510kreport.com/company/mri-devices)
- Philips Medical Systems, Inc.: 3 (https://510kreport.com/company/philips-medical-systems)
- Invivo Research, Inc.: 3 (https://510kreport.com/company/invivo-research)
- Medical Advances, Inc.: 2 (https://510kreport.com/company/medical-advances)
- Medical Data Electronics: 2 (https://510kreport.com/company/medical-data-electronics)
- Oridion, Ltd.: 2 (https://510kreport.com/company/oridion)
- Invivo Therapeutics Corporation: 1 (https://510kreport.com/company/invivo-therapeutics)
- Philips Medizin Systeme Boeblingen GmbH: 1 (https://510kreport.com/company/philips-medizin-systeme-boeblingen)

## Firms that cite its devices most
- Philips Healthcare (Suzhou) Co., Ltd.: 4 (https://510kreport.com/company/philips-healthcare-suzhou)
- Medtronic, Inc.: 2 (https://510kreport.com/company/medtronic)
- Quality Electrodynamics, LLC: 2 (https://510kreport.com/company/quality-electrodynamics)
- Philips Medical Systems Nederland B.V.: 2 (https://510kreport.com/company/philips-medical-systems-nederland)
- Polarean, Inc.: 1 (https://510kreport.com/company/polarean)
- Iradimed Corporation: 1 (https://510kreport.com/company/iradimed)
- Spacelabs Healthcare Medical Equipment (Suzhou) CO: 1 (https://510kreport.com/company/spacelabs-healthcare-medical-equipment-suzhou)
- Neocoil, LLC: 1 (https://510kreport.com/company/neocoil)

## Its most-cited devices
- K153073: UroNav (Version 2.0) (2015), cited by 5
- K090785: Mri Compatible Patient Monitoring System, Model 865214 (2009), cited by 4
- K192200: DynaCAD (2019), cited by 3
- K111673: 1.5T and 3T 8-Channel Medium General Purpose Flex Coil (2011), cited by 3
- K061952: Cardiovascular Array Coils, Models Cac-63-16, Cac-63-32, Cac-123-32 and Cac-127-16 (2006), cited by 3
- K053462: 3160 Mri Patient Monitoring System (2006), cited by 3

## Recent decisions
- K213766: dS FootAnkle 16Ch Coils for 1.5T and 3.0T, dS HiRes HandWrist 16Ch Coils for 1.5T and 3.0T, ds Small Extremity 16Ch Coils for 1.5T and 3.0T (Dec 23, 2021)
- K212227: Philips MR Patient Care Portal (Sep 30, 2021)
- K212175: DynaCAD (Aug 2, 2021)
- K193403: UroNav System (Dec 27, 2019)
- K192200: DynaCAD (Oct 9, 2019)
- K182561: UroNav (Version 3.0) (Oct 19, 2018)
- K162177: dS FootAnkle I6CH 1.5T Coil (Sep 14, 2016)
- K162001: 1.5T and 3.0T 16 CH GE Shoulder Coils (Aug 31, 2016)

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