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Geon Corporation

FDA Regulatory Profile

Geon Corporation appears in FDA public data with 0 recalls, 3 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 4, 2025.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243138Geon (S2) Nasal AspiratorFebruary 4, 2025
K220126Geonic Nasal Aspirator, Geonic Nasal CleanerFebruary 2, 2023
K100563GEON RAPID DIGITAL THERMOMETER MODEL: MT-B117, MT-B127, MT-B130, MT-B132FAJune 2, 2010

FDA data resources