510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K210990Substantially Equivalent

Non-sterile Powder Free Nitrile Examination Gloves

Rubberex Alliance Sdn Bhd, Ipoh, MY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K210990 is the FDA 510(k) clearance record for Non-sterile Powder Free Nitrile Examination Gloves, a class I device, cleared for Rubberex Alliance Sdn Bhd on under FDA product code LZA (Polymer Patient Examination Glove). FDA's definition for product code LZA reads: "A nitrile (or polymer) patient examination glove is a disposable device made of nitrile rubber or synthetic polymers that may or may not bear a trace amount of residual powder, and is intended to be worn on the hand for medical purposes to...". FDA records list one 510(k) clearance for Rubberex Alliance Sdn Bhd. As of , FDA records show no recalls naming K210990.

Clearance record

Decision date
Received
(234 days to decision)
Product code
LZA Polymer Patient Examination Glove
Regulation
21 CFR 880.6250
Device class
Class I
Review panel
General Hospital
Applicant
Rubberex Alliance Sdn Bhd Lot 128201 Off 3/4 Mile, Jalan Bercham, Kawasan, Ipoh, MY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LZA

Trailing 12 months
16 clearances under product code LZA in the twelve months to October 2026, June 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code LZA, trailing twelve months
MonthClearances
November 20251
December 20250
January 20262
February 20260
March 20260
April 20260
May 20260
June 20265
July 20262
August 20261
September 20264
October 20261