ClearanceBrief
Company ยท US

Meditech International, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2008. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
ILYLamp, Infrared, Therapeutic Heating4
NHNPowered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 18, 2008K081355BIOFLEX LD-R100 TREATMENT HEAD
Meditech International, Inc., CA
ILY
Apr 2, 2008K072551LD-I 75 AND LD-I 200
Meditech International, Inc.
NHN
Mar 13, 2006K051875BIOFLEX PRESCRIPTION SYSTEM AND RELATED TREATMENT HEADS
Meditech International, Inc.
ILY
Feb 24, 2005K041885BIOFLEX LD-175 AND LD-1200 TREATMENT HEADS
Meditech International, Inc.
ILY
Apr 10, 2003K023621BIOFLEX PROFESSIONAL THERAPY SYSTEM
Meditech International, Inc.
ILY

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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