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UNIFY Surgical Sutures

FDA UDI

Class II (US FDA UDI)

by Applied Dental, Inc.

Identity

Trade Name
UNIFY Surgical Sutures FDA UDI
Generic Name
Nylon suture, non-bioabsorbable, monofilament FDA UDI
Device Name
Nylon, 3-0, 24mm 3/8 Circle Rev Cut, 30" FDA UDI
Model / Reference
L-N330R24 FDA UDI
Description
Nylon, 3-0, 24mm 3/8 Circle Rev Cut, 30" FDA UDI

Identifiers

Primary DI / UDI-DI
00814639020120 FDA UDI
FDA Product Code
GAR FDA UDI
GMDN Term
Nylon suture, non-bioabsorbable, monofilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5020 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

No

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

Category: Nylon suture, non-bioabsorbable, monofilament

UNIFY Surgical Sutures by Applied Dental, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nylon suture, non-bioabsorbable, monofilament.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Applied Dental, Inc.

Sources (1)

  • FDA UDI 49f16220-adf0-43c1-b116-751e9c523811 34 fields · synced May 31, 2026