PULSEMASTER
K961136 · American Dental Technologies, Inc. · GEX · Jun 3, 1996 · General, Plastic Surgery
Device Facts
| Record ID | K961136 |
| Device Name | PULSEMASTER |
| Applicant | American Dental Technologies, Inc. |
| Product Code | GEX · General, Plastic Surgery |
| Decision Date | Jun 3, 1996 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 878.4810 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Intended Use
The use of the PulseMaster laser for treatment of aphthous ulcers.
Device Story
PulseMaster is a pulsed Nd:YAG dental laser system; used by dental professionals for intraoral soft tissue procedures. Device delivers laser energy to target tissue; facilitates ablation and coagulation. New indication involves treatment of aphthous ulcers; provides immediate pain relief and accelerated healing. Clinical application involves direct laser exposure to lesions; no reported side effects or contraindications. Benefits include immediate palliation and reduced severity of recurrences.
Clinical Evidence
Two studies presented. Study 1: 21 patients (8 aphthous, 14 herpes labialis) followed 6-18 months. Results for aphthous ulcers: 63% reported immediate pain relief, 50% faster healing, 50% no recurrence at 6 months, 75% of remainder reported less severe recurrences. Study 2: 3 case studies; reported immediate pain relief, no discomfort during/after procedure, no side effects.
Technological Characteristics
Pulsed Nd:YAG laser system. Designed for intraoral soft tissue surgical applications including ablation and coagulation.
Indications for Use
Indicated for the treatment of aphthous ulcers in patients suffering from recurrent aphthous ulcers.
Regulatory Classification
Identification
(1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.(2) An argon laser for use in dermatology is a laser device intended to destroy or coagulate tissue by light energy emitted by argon.
Predicate Devices
- PulseMaster laser (legally marketed for coagulation and ablation of intraoral soft tissue)
Related Devices
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- K203396 — DEKA SMARTPERIO · El.En Electronic Engineering Spa · Aug 23, 2021
- K972325 — PULSEMASTER 1000 ST DENTAL LASER SYSTEM · American Dental Technologies, Inc. · Sep 19, 1997
- K961269 — PULSEMASTER · American Dental Technologies, Inc. · Mar 10, 1997
- K030290 — PERIOLASE ND:YAG DENTAL LASER SYSTEM · Millennium Dental Technologies, Inc. · Jul 26, 2004
Submission Summary (Full Text)
{0}
JUN - 3 1996
K961136
American Dental
Technologies
# 510(k) Summary
## Device Name:
Trade Name: PulseMaster
Common Name: Dental Laser System
Classification Name: Surgical Laser System
Indication for Use: Aphthous Ulcers
## Submitter:
American Dental Technologies, Inc.
125 Shoreway Road
Suite 3000
San Carlos, CA 94070
## Contact Person:
Michael Yessik
Tel.: 415-595-7723
Fax: 415-595-3982
## Date Prepared:
March 19, 1996
125 Shoreway Road • Suite 3000 • San Carlos, CA 94070 • (415) 595 7723 Fax (415) 595 3982
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510(k) Summary
This 510(k) Premarket Notification is for a new indication for use for the legally marketed PulseMaster laser family. The use of the PulseMaster laser for treatment of aphthous ulcers is substantially equivalent to the use of the PulseMaster laser for coagulation and ablation of other intraoral soft tissue.
Independent studies have been carried out using a pulsed Nd:YAG laser to treat aphthous ulcers. In one study, 21 patients were treated, eight with recurrent aphthous ulcers and 14 with herpes labialis lesions. The patients were evaluated over a period ranging from six months to eighteen months and the patients were asked to keep a daily calendar over that time period. The study was begun with both treated lesions and untreated, control lesions in each patient. However, all lesions were treated before the end of the study. Results were based on both the investigator’s evaluation at follow-ups and the patient’s self evaluation. For those with aphthous ulcers, immediate relief of pain was reported in 63% of the patients, 50% reported faster healing, 50% had no recurrence within 6 months and 75% of the remaining group reported less severe recurrences. The authors concluded that the pulsed Nd:YAG laser treatment was effective in the control and relief of most aphthous lesions.
In another study using a pulsed Nd:YAG laser for treatment of recurrent aphthous ulcers, three case studies were presented. The patients reported no discomfort during the procedure and no postoperative discomfort or other problems. The patients reported immediate relief of the painful symptoms of the lesions. The authors’ conclusion was that the laser treatment compared favorably with other treatments due to no side effects or contraindications, and immediate palliation of the lesions.
The results of these studies allow the following conclusions:
- The use of the PulseMaster laser for treatment of aphthous ulcers is substantially equivalent to the use of the PulseMaster laser for ablation and coagulation of other intraoral soft tissues.
- There are no new safety risks for this laser procedure.
- The laser treatment for recurrent aphthous ulcers is equivalent to the standard of care for treatment of recurrent aphthous ulcers in terms of effectiveness.