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Menix

FDA UDI

Class II (US FDA UDI)

by S.b.m

Identity

Trade Name
MENIX FDA UDI
Generic Name
Meniscus suture anchor FDA UDI
Device Name
MENIX® system consists of a single-use launcher which deploys a nonabsorbable implant composed of one anchor pre-tied with a suture. FDA UDI
Model / Reference
Meniscal suture system, 1 anchor FDA UDI
Description
MENIX® system consists of a single-use launcher which deploys a nonabsorbable implant composed of one anchor pre-tied with a suture. FDA UDI

Identifiers

Catalog Number
MEN0201902 FDA UDI
Primary DI / UDI-DI
03760304680533 FDA UDI
510(k) Number
K223122 FDA UDI
FDA Product Code
GAT FDA UDI
GMDN Term
Meniscus suture anchor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5000 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Meniscus suture anchor

Menix by S.b.m — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Meniscus suture anchor.

Cleared under the same submission

K223122 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
S.b.m

Sources (1)

  • FDA UDI 99f89312-a725-4687-bce5-1fab2ca6134d 35 fields · synced Jun 8, 2026