Kerr Corporation

11 FDA 510(k) clearances · Recalling firm

Record	Firm	Date
Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The in recall (Z-1788-2014)	Kerr Corporation	2014-06-13
The brand name of the device is Laser Loupes, a dentalloupe with laser eye protection. Las recall (Z-0414-2013)	Kerr Corporation	2012-11-21
BioPlant, a dental bone grafting material. BioPlant has been assigned the product code LYC recall (Z-0401-2013)	Kerr Corporation	2012-11-20
Freedom Cordless LED Light System. Freedom System, Standard Length, Part Number 910863-1, recall (Z-0402-2013)	Kerr Corporation	2012-11-20
The brand name of the device is AlgiNot, a dental impression material. Product Part Number recall (Z-0268-2013)	Kerr Corporation	2012-11-08
Brand Name: TempSpan CMT Temporary Cement, a temporary cement. Part Number: N69CA. The int recall (Z-1205-2012)	Kerr Corporation	2012-03-14
Brand name: Bond-1 Primer/Adhesive, a resin tooth bonding agent. Item # Item Description N recall (Z-1142-2012)	Kerr Corporation	2012-03-02
Brand Name: Fusio Liquid Dentin, part number N21SB, N21SC. Product Usage: The intended use recall (Z-1115-2012)	Kerr Corporation	2012-02-28
Breeze Self-Adhesive Resin Cement, part number: N97F. The intended use is for cementation recall (Z-1100-2012)	Kerr Corporation	2012-02-24
Brand name: Maxcem Elite, Product: a dental cement, Part Number: 34418. The intended use o recall (Z-0915-2012)	Kerr Corporation	2012-01-27
Artiste Maverick Tint, Part Number: N36TB, Lot/Serial Numbers: 3416180, Product Descriptio recall (Z-0455-2012)	Kerr Corporation	2012-01-11

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