Almore Intl., Inc.
Mchenry, IL, US
Almore Intl., Inc. appears in FDA device records in Mchenry, IL. FDA records list 21 510(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
- 21
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 21 510(k) clearances for Almore Intl., Inc. between 1980 and 1986. The busiest year on record is 1986, with 10. The most recent is 1986, with 10.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1981 | 1 |
| 1983 | 9 |
| 1986 | 10 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K862851 | ALMORE FACE MASK | Substantially Equivalent | ||
| K854692 | MONARCH II BLEACHING INSTRUMENT | EEG | Substantially Equivalent | |
| K854696 | OP II VISIBLE LIGHT CURING SYSTEM | EBZ | Substantially Equivalent | |
| K854691 | DIAMOND BURS-HANDPIECE | EJL | Substantially Equivalent | |
| K854690 | DIAMONDS BURS-COMPOSIT FINISHING | EJL | Substantially Equivalent | |
| K854700 | EZ-ON TUBING CONDITIONER (LUBRICANT) | Substantially Equivalent | ||
| K854702 | PLASTIC MOUNTING RINGS | EJP | Substantially Equivalent | |
| K854701 | RETRACT-A-CORD | JES | Substantially Equivalent | |
| K854697 | TUBING HANDPIECE REPLACEMENT | EFB | Substantially Equivalent | |
| K854699 | TUBING SYRING | ECB | Substantially Equivalent | |
| K831136 | DOUBLE BOW TOOTH SEPARATOR | JEP | Substantially Equivalent | |
| K831138 | CURVED HEMOSTAT 5 | HTD | Substantially Equivalent | |
| K831137 | STRAIGHT 5 HEMOSTAT | HTD | Substantially Equivalent | |
| K830776 | MICROFIL CONTOURING INSTRUMENTS | EIY | Substantially Equivalent | |
| K830775 | FACEBOW FOR BALANCE ARTICULATOR | KCR | Substantially Equivalent | |
| K830773 | MARKLEY THREADED WIRE | EBL | Substantially Equivalent | |
| K830878 | BINOCULAR LOUPE | HJH | Substantially Equivalent | |
| K830777 | ELECTRIC MOUTH MIRROR | EAX | Substantially Equivalent | |
| K830774 | BINOCULAR MAGNIFIER 2X | HKC | Substantially Equivalent | |
| K811075 | BALANCE ARTICULATOR | EJP | Substantially Equivalent | |
| K801463 | OJ-1 ENDODONIC ROOT CANAL FILE HOLDER | EKQ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- EBZActivator, Ultraviolet, For Polymerization
- EJPArticulators
- EJLBur, Dental
- KCRFacebow
- JESFloss, Dental
- HTDForceps
- EFBHandpiece, Air-Powered, Dental
- EEGHeat Source For Bleaching Teeth
- EIYInstrument, Filling, Plastic, Dental
- HJHLoupe, Binocular, Low Power
- EAXMirror, Mouth
- EBLPin, Retentive And Splinting, And Accessory Instruments
- EKQPreparer, Root Canal Endodontic
- JEPRetainer, Matrix
- HKCSpectacle Microscope, Low-Vision
- 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