MNUClass II

Staple, Absorbable

21 CFR 888.3030 / Orthopedic

MNU is the FDA product code for Staple, Absorbable, a class II device type, regulated under 21 CFR 888.3030. As of 2026-09-10, FDA records hold 4 510(k) clearances under this code, the most recent dated 2024-08-28, and no recalls.

Classification record

Product code: MNU
Device name: Staple, Absorbable
Regulation: 21 CFR 888.3030
Device class: Class II
Review panel: Orthopedic
Submission type: 510(k)
Implant: Yes
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 4
Ingested recalls: 0

Clearances, product code MNU

By decision year

4 clearances under product code MNU with a decision year between 2001 and 2024, 2001 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code MNU by decision year
Year	Clearances
2001	1
2022	1
2023	1
2024	1

Applicants with the most clearances

Product code MNU

Applicants holding the most 510(k) clearances under product code MNU
Applicant	Clearances
OSSIO, Ltd.	3
Arthrex GmbH	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 13 companies shown, in name order

Recent clearances

Product code MNU

Recent recalls

Product code MNU

FDA records show no recalls under product code MNU.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)