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Hexa

FDA UDI

Class II (US FDA UDI)

by Hexa Dental

Identity

Trade Name
Hexa FDA UDI
Generic Name
Nylon suture, bioabsorbable, antimicrobial FDA UDI
Device Name
PGA Undyed Suture FDA UDI
Model / Reference
HPGA-57754U FDA UDI
Description
PGA Undyed Suture FDA UDI

Identifiers

Catalog Number
HPGA-57754U FDA UDI
Primary DI / UDI-DI
00850023750129 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Nylon suture, bioabsorbable, 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

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

Yes

FDA UDI

Category: Nylon suture, bioabsorbable, antimicrobial

Hexa by Hexa Dental — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nylon suture, bioabsorbable, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hexa Dental

Sources (1)

  • FDA UDI 3ef994cd-90c4-470a-a040-7b4b43bad7f7 35 fields · synced May 30, 2026