Pacific Dental Corp.
Mchenry, IL, US
Pacific Dental Corp. appears in FDA device records in Mchenry, IL. FDA records list 22 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 22
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 22 510(k) clearances for Pacific Dental Corp. between 1980 and 1982. The busiest year on record is 1982, with 15. The most recent is 1982, with 15.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 7 |
| 1982 | 15 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K821782 | BEACH ANESTHETIC SYRINGE CARTR. TYPE | EJI | Substantially Equivalent | |
| K821790 | BEACH EXCAVATOR'S NO. 1 & NO. 2 | EKD | Substantially Equivalent | |
| K821789 | BEACH CURETTE NO. 2 AND NO. 3 T.G. | EMS | Substantially Equivalent | |
| K821788 | BEACH DERIOSTEAL ELEVATOR, #2 STRAIGHT | EMJ | Substantially Equivalent | |
| K821787 | BEACH SURGICAL PLIERS NON-HOOK | EJY | Substantially Equivalent | |
| K821786 | BEACH SCALERS | EMN | Substantially Equivalent | |
| K821785 | BEACH AMALGAM CARVER | EKH | Substantially Equivalent | |
| K821784 | BEACH GINGIVAL RETRACTION INSTR. TYPE B | EIG | Substantially Equivalent | |
| K821783 | BEACH SILICATE FILLING & LINING APPLIC. | Substantially Equivalent | ||
| K821780 | BEACH EXPLORER NO. 23T.G. | EKB | Substantially Equivalent | |
| K821779 | BEACH AMALGAM CARRIER, GUN TYPE | EKJ | Substantially Equivalent | |
| K821778 | BEACH DRESSING PLIER | EFL | Substantially Equivalent | |
| K821777 | BEACH MOUTH MIRROR | EAX | Substantially Equivalent | |
| K821781 | BEACH FORCEP NO. 150 AND NO. 151 | EMG | Substantially Equivalent | |
| K821739 | J. MORITA FLEX M-3 TORX HARDPIECE | EKX | Substantially Equivalent | |
| K801688 | TORX HANDPIECE CONTRA ANGLES ATTACHMENTS | EGS | Substantially Equivalent | |
| K801687 | TORX MICRO-MOTOR LOW SPEED HANDPIECE | EKX | Substantially Equivalent | |
| K801686 | SPACELINE THREE WAY SYRINGE | ECB | Substantially Equivalent | |
| K801685 | SPACELINE DENTAL CHAIR-UNIT | EIA | Substantially Equivalent | |
| K801684 | ASTRON AIR POWERED HIGH SPEED DE PIECE | Substantially Equivalent | ||
| K801683 | LUNA-VUE DENTAL OPERATING LIGHT | EAZ | Substantially Equivalent | |
| K801682 | SPACELINE HIGH VOLUME EVACUATION HANDPIE | EHZ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- EKJBurnisher, Operative
- EKHCarver, Dental Amalgam, Operative
- EMSCurette, Periodontic
- EMJElevator, Surgical, Dental
- EHZEvacuator, Oral Cavity
- EKBExplorer, Operative
- EFLForceps, Dressing, Dental
- EMGForceps, Tooth Extractor, Surgical
- EGSHandpiece, Contra- And Right-Angle Attachment, Dental
- EKXHandpiece, Direct Drive, Ac-Powered
- EKDInstrument, Cutting, Operative
- EAZLight, Operating, Dental
- EAXMirror, Mouth
- EJYPliers, Operative
- EIGRetractor, All Types
- EMNScaler, Periodontic
- EJISyringe, Cartridge
- EIAUnit, Operative Dental
- ECBUnit, Syringe, Air And/Or Water
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain