Browse hierarchy: [Dental (DE)](/submissions/DE) → [Subpart D — Prosthetic Devices](/submissions/DE/subpart-d%E2%80%94prosthetic-devices) → [21 CFR 872.3150](/submissions/DE/subpart-d%E2%80%94prosthetic-devices/872.3150) → EJP — Articulators

# EJP · Articulators

_Dental · 21 CFR 872.3150 · Class 1_

**Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP

## Overview

- **Product Code:** EJP
- **Device Name:** Articulators
- **Regulation:** [21 CFR 872.3150](/submissions/DE/subpart-d%E2%80%94prosthetic-devices/872.3150)
- **Device Class:** 1
- **Review Panel:** [Dental](/submissions/DE)
- **GMP exempt:** yes

## Identification

An articulator is a mechanical device intended to simulate movements of a patient's upper and lower jaws. Plaster casts of the patient's teeth and gums are placed in the device to reproduce the occlusion (bite) and articulation of the patient's jaws. An articulator is intended to fit dentures or provide orthodontic treatment.

## Classification Rationale

Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 872.9. If the device is not labeled or otherwise represented as sterile, the device is exempt from the current good manufacturing practice requirements of the quality management system regulation in part 820 of this chapter, except for requirements concerning records and complaint files under § 820.35 of this chapter.

## Recent Cleared Devices (11 of 11)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [K926190](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K926190.md) | ALRAND INC. (DENTAL HAND INSTRUMENTS) | Alrand, Inc. | Jan 18, 1994 | SESE |
| [K896131](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K896131.md) | GNATHOMAT ARTICULATOR | Ivoclar North America, Inc. | Dec 4, 1989 | SESE |
| [K892373](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K892373.md) | DENTAL PLASTIC BITE FORK | Texapol Corp. | Jun 12, 1989 | SESE |
| [K884418](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K884418.md) | PREMIER DIE-TRAK ARTICULATOR | Premier Medical | Nov 14, 1988 | SESE |
| [K872943](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K872943.md) | DISPOSABLE ARTICULATOR | Dentsply Intl. | Aug 11, 1987 | SESE |
| [K863009](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K863009.md) | GNATUS ARTICULATOR 4.300/4.300GP 8.600 & ORTOFLEX | Sds Dental, Inc. | Sep 25, 1986 | SESE |
| [K854702](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K854702.md) | PLASTIC MOUNTING RINGS | Almore Intl., Inc. | Mar 6, 1986 | SESE |
| [K833039](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K833039.md) | HANDY IIM | Shofu Dental Corp. | Oct 4, 1983 | SESE |
| [K811075](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K811075.md) | BALANCE ARTICULATOR | Almore Intl., Inc. | May 13, 1981 | SESE |
| [K810971](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K810971.md) | THE GNATOMET | Bauer, Cheng & Associates, Inc. | May 5, 1981 | SESE |
| [K801342](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP/K801342.md) | DISPOSABLE ARTICULATOR | Williams Gold Refining Co., Inc. | Jul 8, 1980 | SESE |

## Top Applicants

- Almore Intl., Inc. — 2 clearances
- Alrand, Inc. — 1 clearance
- Bauer, Cheng & Associates, Inc. — 1 clearance
- Dentsply Intl. — 1 clearance
- Ivoclar North America, Inc. — 1 clearance

---

**Source:** [https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJP)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com