← Back to catalogue

Adjustable Depth Stop

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
ADJUSTABLE DEPTH STOP FDA UDI
Generic Name
Surgical depth gauge, reusable FDA UDI
Device Name
ADJUSTABLE DEPTH STOP FDA UDI
Model / Reference
324-0011 FDA UDI
Description
ADJUSTABLE DEPTH STOP FDA UDI

Identifiers

Catalog Number
324-0011 FDA UDI
Primary DI / UDI-DI
00810189110397 FDA UDI
510(k) Number
K230764 FDA UDI
FDA Product Code
HTJ FDA UDI
GMDN Term
Surgical depth gauge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4300 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical depth gauge, reusable

Adjustable Depth Stop by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical depth gauge, reusable.

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 008358e3-ea2e-4379-a968-029bc72916dc 36 fields · synced Jun 1, 2026