Glypto Device, Glypto Cryo Machine;
Official notice from a government agency or its published feed.
Glypto Device, Glypto Cryo Machine;
Reason: Lack of 510(k) clearance.
Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide distribution.
Reason: Lack of 510(k) clearance.
Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide distribution.
Hazard: Lack of 510(k) clearance.
View the FDA enforcement report ↗ ← All reports