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Techfit

FDA UDI

Class II (US FDA UDI)

by Techfit Digital Surgery, Inc.

Identity

Trade Name
TECHFIT FDA UDI
Generic Name
Custom-made orthopaedic/craniofacial surgical guide FDA UDI
Device Name
Genioplasty Surgical Guide - Resin FDA UDI
Model / Reference
0 FDA UDI
Description
Genioplasty Surgical Guide - Resin FDA UDI

Identifiers

Catalog Number
GCGBC FDA UDI
Primary DI / UDI-DI
00860010801604 FDA UDI
510(k) Number
K230276 FDA UDI
FDA Product Code
DZJ FDA UDI
LLZ FDA UDI
GMDN Term
Custom-made orthopaedic/craniofacial surgical guide FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4120 FDA UDI
892.2050 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

Category: Custom-made orthopaedic/craniofacial surgical guide

Techfit by Techfit Digital Surgery, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Custom-made orthopaedic/craniofacial surgical guide.

Cleared under the same submission

K230276 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Techfit Digital Surgery, Inc.

Sources (1)

  • FDA UDI 440ced1c-a482-480c-8520-aeaef350cb9a 35 fields · synced May 30, 2026