510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K133507Substantially Equivalent

Guidoss

Nibec Co., Ltd., Los Angeles CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K133507 is the FDA 510(k) clearance record for GUIDOSS, a class II device, cleared for Nibec Co., Ltd. on under FDA product code NPL (Barrier, Animal Source, Intraoral). FDA's definition for product code NPL reads: "An animal source dental barrier is an animal-derived material device, such as collagen, intended to aid in guided tissue/bone regeneration procedures and to act as a stable barrier for the containment of bone graft materials when placed...". FDA records list 2 510(k) clearances for Nibec Co., Ltd., from to . As of , FDA records show no recalls naming K133507.

Clearance record

Decision date
Received
(356 days to decision)
Product code
NPL Barrier, Animal Source, Intraoral
Regulation
21 CFR 872.3930
Device class
Class II
Review panel
Dental
Applicant
Nibec Co., Ltd. 4568 W. 1st St. Suite 104, Los Angeles CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NPL

Trailing 12 months
3 clearances under product code NPL in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code NPL, trailing twelve months
MonthClearances
November 20251
December 20252
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260