Terarecon,Inc.
Terarecon,Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2025, with 1 FDA device recall on record.
Top product codes for Terarecon,Inc.
FDA recalls by Terarecon,Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Terarecon,Inc.
- K250288 — TeraRecon Cardiovascular.Calcification.CT
- K243158 — TeraRecon Aorta.CT (1.1.0)
- K241312 — TeraRecon Cardiac.Chambers.MR (1.0.0)
- K220349 — TeraRecon Neuro
- K200750 — Neuro.Al Algorithm
- K191585 — iNtuition-Structural Heart Module
- K180916 — iNtuition-T1 Mapping and T2/T2* Mapping
- K131447 — INTUITION - TDA, TVA, PARAMETRIC MAPPING
- K121916 — INTUITION
- K061214 — AQUARIUSAPS SERVER
- K012086 — AQUARIUSNET SERVER
- K011142 — AQUARIUS WORKSTATION
- K994329 — IIVS INTEGRATED IMAGE VIEWING STATION
- K974307 — RTR-2000/RTR-4000
Data sourced from openFDA. This site is unofficial and independent of the FDA.