510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K102119Substantially Equivalent

Sur-G Glov and Maxitex

Terang Nusa (Malaysia) Sdn. Bhd., Kota Bharu, Kelantan, MY / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K102119 is the FDA 510(k) clearance record for SUR-G GLOV AND MAXITEX, a class I device, cleared for Terang Nusa Sdn Bhd on under FDA product code KGO (Surgeon'S Gloves). FDA's definition for product code KGO reads: "A surgeon's glove is a disposable device made of natural rubber latex or synthetic polymers that may or may not bear powder to facilitate donning, and it is intended to be worn on the hands, usually in surgical settings, to provide a...". FDA records list 26 510(k) clearances for TERANG NUSA (MALAYSIA) SDN. BHD., from to . As of , FDA records show no recalls naming K102119.

Clearance record

Decision date
Received
(30 days to decision)
Product code
KGO Surgeon'S Gloves
Regulation
21 CFR 878.4460
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Terang Nusa Sdn Bhd 1, Jalan 8,, Kota Bharu, Kelantan, MY
510(k) summary
Statement
Third party review
No

Clearances, product code KGO

Trailing 12 months
2 clearances under product code KGO in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KGO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20261
August 20260
September 20260
October 20260