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Alphamed, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K190210
Tear Pool Dissolvable Punctum Plugs
October 24, 2019
K091240
ALPHAMED SURGICAL SPEAR, MODEL 70-5000
October 23, 2009
K990321
ALPHAMED GEMINI SENSOR, SNORING SENSOR
June 1, 1999
K926446
EZ PUMP
September 27, 1993