Interpore Intl.
Walker, MI, US
Interpore Intl. appears in FDA device records in Walker, MI. FDA records list 25 510(k) clearances between and , 12 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
- 25
- PMA records
- 12
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 25 510(k) clearances for Interpore Intl. between 1984 and 1998. The busiest year on record is 1984, with 3. The most recent is 1998, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 3 |
| 1986 | 3 |
| 1987 | 1 |
| 1988 | 1 |
| 1990 | 2 |
| 1991 | 1 |
| 1992 | 3 |
| 1994 | 2 |
| 1995 | 2 |
| 1996 | 3 |
| 1997 | 2 |
| 1998 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K981253 | ULTRACON ULTRAFILTRATOR | FJI | Substantially Equivalent | |
| K980817 | PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L | MQV | Substantially Equivalent | |
| K972842 | INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE | LYC | Substantially Equivalent | |
| K971036 | ODONTIT AUTOGENOUS BONE COLLECTION DEVICE | GCY | Substantially Equivalent | |
| K960945 | IMZ MEMBRANE TACK SYSTEM | DZL | Substantially Equivalent | |
| K960371 | INTERPORE THREADED IMPLANT | DZE | Substantially Equivalent | |
| K955492 | INTERPORE IMZ CYL IMPLANT & CYL HEX IMPLT | DZE | Substantially Equivalent | |
| K952167 | IMZ BONE TACK SYSTEM | DZL | Substantially Equivalent | |
| K950165 | INTERPORE IP 200 GRANULAR CORALLINE HYDROXYAPATITE BONE VOID FILLERS, 425 TO 1000 MICRONS AND 425 TO 600 MICRONS | LYC | Substantially Equivalent | |
| K922872 | INTERPORE CYLINDRICAL HEX HYDROXYAPATITE COATED IMPLANT, 3.3 MM DIAM. | DZE | Substantially Equivalent | |
| K922732 | INTERPORE CYLINDRICAL HEX IMPLANT, 3.3 MM DIAMETER | DZE | Substantially Equivalent | |
| K913228 | INTERPORE IMZ CYLINDER IMPLANT SYSTEM | DZE | Substantially Equivalent | |
| K921246 | IMZ SURGICAL INSTRUMENT TRAY | DZE | Substantially Equivalent | |
| K912734 | INTERPORE HEX HEAD IMPLANT RESTORATIVE COMPONENTS | DZE | Substantially Equivalent | |
| K904611 | INTERPORE CYLINDRICAL HEX IMPLANT | DZE | Substantially Equivalent | |
| K900793 | INTERPORE IMZ SINGLE TOOTH ATTACHMENT SYSTEM | DZE | Substantially Equivalent | |
| K901928 | INTERPORE IMZ(CASTABLE)TUB/SCRET RET RIGID ATTACH | EGG | Substantially Equivalent | |
| K883211 | IMZ O-RING ATTACHMENT | DZE | Substantially Equivalent | |
| K870331 | IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS | EGG | Substantially Equivalent | |
| K863680 | IMZ INTRAMOBILE CYLINDER IMPLANT SYSTEM COMPONENTS | DZE | Substantially Equivalent | |
| K860983 | INTERPORE 200 POROUS HYDROXYAPATITE | LYC | Substantially Equivalent | |
| K855032 | IMZ INTRAMOBILE CYLINDER IMPLANT | DZE | Substantially Equivalent | |
| K843154 | TOOTH ROOT SOCKET GAUGE | LYC | Substantially Equivalent | |
| K843153 | ANTERIOR ALVEOLAR RIDGE SIZER | LYC | Substantially Equivalent | |
| K841201 | POROUS HYDROXYAPATITE BG200 | LYC | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GCYApparatus, Suction, Single Patient Use, Portable, Nonpowered
- EGGAttachment, Precision, All
- LYCBone Grafting Material, Synthetic
- OISCalcium Salt Bone Void Filler, Drillable, Non-Screw Augmentation
- FJIDialyzer, Capillary, Hollow Fiber
- MQVFiller, Bone Void, Calcium Compound
- MBSFiller, Bone Void, Non-Osteoinduction
- DZEImplant, Endosseous, Root-Form
- DZLScrew, Fixation, Intraosseous
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.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Interpore Intl. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Interpore Intl.. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.
Data as of , FDA export datePage updated Source: openFDA, public domain