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JEP

3 FDA 510(k) clearances · Product code

FDA profile

Official device name
Retainer, Matrix
Device class
Class I (low risk)
Regulation
21 CFR 872.4565
Medical specialty
Dental
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RecordFirmDate
SLICKS SECTIONAL MATRIX AND MATRIX BANDS, MODELS SM100, SM150, SM175, SM200, SM300, SMH100, SMH150, SMH175 AND SMH200 (K091533)Garrison Dental Solutions2009-08-17
OMNI-MATRIX (K930151)Innovative Technology , Ltd.1993-09-23
DOUBLE BOW TOOTH SEPARATOR (K831136)Almore Intl., Inc.1983-06-08

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Every clearance here is in the API, with alerts when new ones post.