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U.S. IOL, Inc.

FDA UDI

Class II (US FDA UDI)

by U.S. Iol, Inc.

Identity

Trade Name
U.S. IOL, Inc. FDA UDI
Generic Name
Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI
Device Name
9/0 Micro Spatula, Double-Armed PGA Suture FDA UDI
Model / Reference
US-9002LZV FDA UDI
Description
9/0 Micro Spatula, Double-Armed PGA Suture FDA UDI

Identifiers

Catalog Number
US-9002LZV FDA UDI
Primary DI / UDI-DI
00814106016120 FDA UDI
510(k) Number
K140039 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4493 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Polyester suture, bioabsorbable, monofilament, non-antimicrobial

U.S. IOL, Inc. by U.S. Iol, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyester suture, bioabsorbable, monofilament, non-antimicrobial.

Cleared under the same submission

K140039 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
U.S. Iol, Inc.

Sources (1)

  • FDA UDI 478d8095-69ab-40cc-b254-19a0e16475d8 37 fields · synced May 29, 2026