Dynarex L-Mesitran Soft

FDA UDI

Class U (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name: Dynarex L-Mesitran Soft FDA UDI
Generic Name: Medical honey liquid barrier dressing FDA UDI
Model / Reference: 3078 FDA UDI

Identifiers

Primary DI / UDI-DI: 00616784307831 FDA UDI
510(k) Number: K150676 FDA UDI
FDA Product Code: FRO FDA UDI
GMDN Term: Medical honey liquid barrier dressing FDA UDI

Classification

Device Class: U FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical honey liquid barrier dressing

Dynarex L-Mesitran Soft by Dynarex Corp. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical honey liquid barrier dressing.

MEDIHONEY® — ACELL, INC. · U
L-Mesitran Tulle — Theo Manufacturing B.V. · U
MediHoney® — ACELL, INC. · U
Dr.Med — Roosin Medical Co., Ltd. · Class I
L-Mesitran Soft 1.75oz — Theo Manufacturing B.V. · U
MEDLINE — MEDLINE INDUSTRIES, INC. · U
CVS Health® — WOONSOCKET PRESCRIPTION CENTER, INCORPORATED · U
CVS Health® — WOONSOCKET PRESCRIPTION CENTER, INCORPORATED · U

Cleared under the same submission

K150676 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class U	Pending data

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Manufacturer

Manufacturer: Dynarex Corp.

Sources (1)

FDA UDI 0c4e9c1e-556d-4d01-8b05-2dfaee746836 33 fields · synced May 31, 2026