← Back to catalogue

Surgical Instrument

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref SPGUModel INSTRUMENTS CLASS I

by S.I.N. - Sistema DE Implante Nacional S.A.

Identity

Trade Name
DEPTH PROBE GUIDED EUDAMED
SURGICAL INSTRUMENT FDA UDI
Generic Name
Dental implantation depth/angle gauge, reusable FDA UDI
Device Name
DEPTH PROBE EUDAMED
GUIDED DEPTH PROBE FDA UDI
Model / Reference
SPGU EUDAMEDFDA UDI
INSTRUMENTS CLASS I EUDAMED
Description
GUIDED DEPTH PROBE FDA UDI

Identifiers

Catalog Number
SPGU FDA UDI
Primary DI / UDI-DI
07899995298799 EUDAMEDFDA UDI
Basic UDI-DI
999520000021JN EUDAMED
510(k) Number
K201688 FDA UDI
FDA Product Code
KCT FDA UDI
EMDN Code
L159099 ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Dental implantation depth/angle gauge, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Market of Registration
Portugal EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implantation depth/angle gauge, reusable

Surgical Instrument by S.I.N. - Sistema DE Implante Nacional S.A. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation depth/angle gauge, reusable.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI a7ec0b7f-406a-4c67-b32c-81aacd82dc0a 35 fields · synced Oct 9, 2026
  • EUDAMED 27dcbbd3-b462-4dff-9f66-a5c8dff4978d 61 fields · synced Oct 9, 2026