← Back to catalogue

Hexagon

FDA UDI

Class II (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
Hexagon FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
HEXAGON NP Implant, Ø 3.7 mm/3.5 mm, L 13.0 mm; incl. Sterile Cover Screw FDA UDI
Model / Reference
1312007 FDA UDI
Description
HEXAGON NP Implant, Ø 3.7 mm/3.5 mm, L 13.0 mm; incl. Sterile Cover Screw FDA UDI

Identifiers

Catalog Number
1312007 FDA UDI
Primary DI / UDI-DI
00614950015559 FDA UDI
510(k) Number
K102981 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 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

Dimensions & Sizes

Size
Outer Diameter — 3.7 Millimeter FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Hexagon by Ace Surgical Supply Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 7e4cc5b1-423d-49eb-874b-1d124c4b9a03 37 fields · synced May 30, 2026