Maytex Corp.

Maytex Corp. holds 4 FDA 510(k) medical device clearances, first cleared 1989, most recent 1994, with 1 FDA device recall on record.

FDA recalls by Maytex Corp.

Z-1451-2013 — Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is manufactured and distributed by Maytex Corporation, CA Ear-loop face mask for basic medical/dental procedures.Class II·Terminated·2013-05-15

Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.

Recent clearances by Maytex Corp.

K935314 — MAYTEX LATEX EXAMINATION GLOVES, POWDEREDCode LYY·1994-08-01
K935315 — MAYTEX POWDER-FREE LATEX EXAMINATION GLOVESCode LYY·1994-08-01
K892082 — MAYTEX NON-STERILE LATEX EXAM GLOVESCode LYY·1989-05-31
K892183 — MAYTEX LATEX EXAMINATION GLOVESCode LYY·1989-05-31

Data sourced from openFDA. This site is unofficial and independent of the FDA.

Top product codes for Maytex Corp.

FDA recalls by Maytex Corp.

Recent clearances by Maytex Corp.