Ultimate Wireforms, Inc.
Bristol, CT, US
ULTIMATE WIREFORMS, INC. appears in FDA device records in Bristol, CT. FDA records list 6 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 6 510(k) clearances for Ultimate Wireforms, Inc. between 1992 and 1996. The busiest year on record is 1992, with 3. The most recent is 1996, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1992 | 3 |
| 1993 | 2 |
| 1996 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K960799 | ORTHO-ICE | EAT | Substantially Equivalent | |
| K924805 | ORTHODONTIC ARCH WIRE | DZC | Substantially Equivalent | |
| K923837 | DIMPLED MULTI MODULUS ARCH WIRE | DZC | Substantially Equivalent | |
| K923836 | .016' X .016 NICKEL TITANIUM UPRIGHTING SPRING | DZC | Substantially Equivalent | |
| K923838 | THE ULTIMATE RCS ARCH WIRE | DZC | Substantially Equivalent | |
| K923839 | NITINOL GENTLE TOUCH COIL SPRING | DZC | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1221844 | 1221844 | ULTIMATE WIREFORMS, INC. | 200 CENTRAL ST., Bristol, CT 06010 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain