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Hu-Friedy Mfg Co, Inc.

8 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Dental Explorer #2 D/E, Mfr. Part Code/Product Code 101-0913, distributed under the Henry recall (Z-0526-05)Hu-Friedy Mfg Co, Inc.2005-02-04
Dental Explorer #23 S/E, Mfr. Part Code/Product Code 100-3620, distributed under the Henry recall (Z-0527-05)Hu-Friedy Mfg Co, Inc.2005-02-04
Dental Explorer D/E #5, Mfr. Part Code/Product Code 100-8008, distributed under the Henry recall (Z-0528-05)Hu-Friedy Mfg Co, Inc.2005-02-04
Dental Explorer Single End #7, Mfr. Part Code/Product Code 100-7409. Distributed under the recall (Z-0529-05)Hu-Friedy Mfg Co, Inc.2005-02-04
HENRY SCHEIN(R) 101-0913 Explorer #2 D/E. Barcode *+H658101091306*. Made in China. For pro recall (Z-0832-04)Hu-Friedy Mfg Co, Inc.2004-07-20
HENRY SCHEIN(R) 100-3620 Explorer-Single End #23 SE. Barcode *+H658100362003*. Made in Chi recall (Z-0833-04)Hu-Friedy Mfg Co, Inc.2004-07-20
HENRY SCHEIN(R) 100-8008 Explorer-Double End #5. Barcode *+H658100800808*. Made in China. recall (Z-0834-04)Hu-Friedy Mfg Co, Inc.2004-07-20
Non-Sterile Suture Needles, Reverse Cutting, 1/2 Circle, Stainless Steel; 12 suture needle recall (Z-0802-03)Hu-Friedy Mfg Co, Inc.2003-05-09

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