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Shinemound Enterprise, Inc.

8 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
POWDERED LATEX PATIENT EXAMINATION GLOVES (K051913)Shinemound Enterprise, Inc.2005-09-30
SENSI-PRO, DISPOSABLE PRE-POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES WITH BEIGE PIGMENT ADDITIVES (K994248)Shinemound Enterprise, Inc.2000-01-28
SENSI-PRO DISPOSABLE POWDER FREE SYNTHETIC VINYL PATIENT EXAMINATION GLOVES WITH BEIGE PIGMENT ADDITIVES (K994258)Shinemound Enterprise, Inc.2000-01-20
SENSI-PRO DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES (K993240)Shinemound Enterprise, Inc.1999-10-27
SENSI-PRO DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE PIGMENT ADDITIVES (K993231)Shinemound Enterprise, Inc.1999-10-27
SYNTEX (K971360)Shinemound Enterprise, Inc.1997-12-22
LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES (K972104)Shinemound Enterprise, Inc.1997-08-15
POLY-MED (K970625)Shinemound Enterprise, Inc.1997-03-27

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