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Salvin Dental Specialties

FDA UDI

Class II (US FDA UDI)

by Salvin Dental Specialties, Llc

Identity

Trade Name
Salvin Dental Specialties FDA UDI
Generic Name
Craniofacial bone screw, non-bioabsorbable FDA UDI
Device Name
Wide Extraction Screw For Benex Pro Atraumatic Extraction Kit - 2.1mm x 16mm FDA UDI
Model / Reference
MEIS-BE001-230-085 FDA UDI
Description
Wide Extraction Screw For Benex Pro Atraumatic Extraction Kit - 2.1mm x 16mm FDA UDI

Identifiers

Catalog Number
MEIS-BE001-230-085 FDA UDI
Primary DI / UDI-DI
00841336120891 FDA UDI
510(k) Number
K073342 FDA UDI
FDA Product Code
DZL FDA UDI
GMDN Term
Craniofacial bone screw, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4880 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Craniofacial bone screw, non-bioabsorbable

Salvin Dental Specialties by Salvin Dental Specialties, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial bone screw, non-bioabsorbable.

Cleared under the same submission

K073342 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Salvin Dental Specialties, Llc

Sources (1)

  • FDA UDI 2324db65-1a13-41e3-b139-b2ce8f3afc7d 35 fields · synced Jun 8, 2026