510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K163267Substantially Equivalent

Nitrile Examination Glove

Brightway Holdings Sdn. Bhd., Klang, MY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K163267 is the FDA 510(k) clearance record for NITRILE EXAMINATION GLOVE, a class I device, cleared for Brightway Holdings 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 24 510(k) clearances for Brightway Holdings Sdn. Bhd., from to . As of , FDA records show no recalls naming K163267.

Clearance record

Decision date
Received
(123 days to decision)
Product code
LZA Polymer Patient Examination Glove
Regulation
21 CFR 880.6250
Device class
Class I
Review panel
General Hospital
Applicant
Brightway Holdings Sdn. Bhd. Lot 1559, Jalan Istimewa, Batu Belah, Klang, MY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LZA

Trailing 12 months
15 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 20260