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GoldenDent

FDA UDI

Class II (US FDA UDI)

by GoldenDent

Identity

Trade Name
GoldenDent FDA UDI
Generic Name
Suturing unit, single-use FDA UDI
Device Name
Coated Polyglycolic Acid (PGA) Braided Absorbable Suture Violet, 3-0, 19mm, 3/8 reverse cutting needle, Qty 12 FDA UDI
Model / Reference
SPGA3 FDA UDI
Description
Coated Polyglycolic Acid (PGA) Braided Absorbable Suture Violet, 3-0, 19mm, 3/8 reverse cutting needle, Qty 12 FDA UDI

Identifiers

Catalog Number
SPGA3 FDA UDI
Primary DI / UDI-DI
00850028211465 FDA UDI
510(k) Number
K073614 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Suturing unit, single-use 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suturing unit, single-use

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

Similar devices

Also classified as Suturing unit, 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
GoldenDent

Sources (1)

  • FDA UDI 94cdbef3-edcd-4632-96cc-a05ea933c06c 35 fields · synced May 31, 2026