FDA applicant
Advanced Medical Technologies AG
FDA records 11 decisions for Advanced Medical Technologies AG (Round Rock, TX) from 2004 to 2012: 11 510(k) clearances. Most are in product codes MAX (Intervertebral Fusion Device With Bone Graft…) and KWQ (Appliance, Fixation, Spinal Intervertebral Body). Its devices cite 19 predicates, 2 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Advanced Medical Technologies, Inc.”, “Advanced Medical Technologies”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Advanced Medical Technologies AG’s devices, and how often a recall has named them.
FDA decisions per year
4in 2012
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Advanced Medical Technologies AG’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report