← Back to catalogue

OptimalHT™

FDA UDI

Class II (US FDA UDI)

by Forma Medical, Inc.

Identity

Trade Name
OptimalHT™ FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, single-use FDA UDI
Device Name
Distal Sleeve, MIS Targeting Instrument FDA UDI
Model / Reference
6100.1103 FDA UDI
Description
Distal Sleeve, MIS Targeting Instrument FDA UDI

Identifiers

Catalog Number
6100.1103 FDA UDI
Primary DI / UDI-DI
00810136430882 FDA UDI
510(k) Number
K230945 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, 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

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic prosthesis implantation positioning instrument, 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 prosthesis implantation positioning instrument, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Forma Medical, Inc.

Sources (1)

  • FDA UDI 79e5ee70-2a2c-4624-bfcd-13c14709864b 36 fields · synced Jun 8, 2026