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TekBrace Solo

FDA UDI

Class II (US FDA UDI)

by Theramicro

Identity

Trade Name
TekBrace Solo FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
Soft Tissue Reinforcement Device - 12cm FDA UDI
Model / Reference
2470S012 FDA UDI
Description
Soft Tissue Reinforcement Device - 12cm FDA UDI

Identifiers

Primary DI / UDI-DI
00810198920055 FDA UDI
510(k) Number
K251063 FDA UDI
FDA Product Code
QUW FDA UDI
FTL FDA UDI
OWX FDA UDI
GMDN Term
Polyester suture, non-bioabsorbable, multifilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Polyester suture, non-bioabsorbable, multifilament

TekBrace Solo by Theramicro — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyester suture, non-bioabsorbable, multifilament.

Cleared under the same submission

K251063 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Theramicro

Sources (1)

  • FDA UDI bbb4045d-1779-4188-8980-a2f4f5383927 34 fields · synced May 30, 2026