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Syntec Internal Hex Captured Screw

FDA UDI

Class II (US FDA UDI)

by Syntec Scientific Corp.

Identity

Trade Name
Syntec Internal Hex Captured Screw FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, non-sterile FDA UDI
Device Name
Syntec Internal Hex Captured Screw φ5.0 x L60mm FDA UDI
Model / Reference
S880067 FDA UDI
Description
Syntec Internal Hex Captured Screw φ5.0 x L60mm FDA UDI

Identifiers

Primary DI / UDI-DI
04712782906918 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, non-sterile 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, non-sterile

Syntec Internal Hex Captured Screw by Syntec Scientific Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Syntec Scientific Corp.

Sources (1)

  • FDA UDI 300bd72c-898c-492b-8b70-4835e4be0b9f 33 fields · synced Jun 1, 2026