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OptimalHT™

FDA UDI

Class II (US FDA UDI)

by Forma Medical, Inc.

Identity

Trade Name
OptimalHT™ FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
0.9mm K-wires, Stainless Steel, 6” Long FDA UDI
Model / Reference
6100.2609 FDA UDI
Description
0.9mm K-wires, Stainless Steel, 6” Long FDA UDI

Identifiers

Catalog Number
6100.2609 FDA UDI
Primary DI / UDI-DI
00810136430899 FDA UDI
510(k) Number
K230945 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic guidewire, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.9 Millimeter FDA UDI
Length — 152 Millimeter FDA UDI

Category: Orthopaedic guidewire, single-use

OptimalHT™ by Forma Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Forma Medical, Inc.

Sources (1)

  • FDA UDI 831ef594-81ed-488f-aab8-53d9affca961 36 fields · synced May 30, 2026